http://identifiers.org/hco/10/GRCh38#22928118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#19204198-C-A

22928118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19204198-C-T

22928209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19204281-G-T

22928251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19204318-G-A

22928251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 19204318-G-T

22928825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19204818-C-T

22930172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19205384-C-T

22930459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19205794-G-A

22930459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19205794-G-C

22930535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19205949-C-G

22930535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19205949-C-T

22931951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206528-G-A

22931951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206528-G-T

22932033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19206615-C-G

22932033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 19206615-C-T

http://identifiers.org/hco/10/GRCh38#22932072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19206654-C-A

22932075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206657-T-A

22932075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206657-T-C

22932078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206660-A-G

22932118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206700-A-G

22932144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206726-G-A

22932144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206726-G-T

22932283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206862-G-A

22932292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206871-T-C

22932352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19206932-G-T

22932493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19207060-G-A

http://identifiers.org/hco/10/GRCh38#22932588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19207160-C-A

22933097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19207613-T-C

22933235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19207757-A-G

22933328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19207831-G-A

22933563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19208120-T-G

22934204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19238353-C-T

22934406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19238530-T-A

22934413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19238537-C-G

22934476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19238577-T-A

22934757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19238851-T-C

22936528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19239217-A-G

22936742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19239442-T-A

22936766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19239466-G-A

22946046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19240202-G-A

22946046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19240202-G-T

22946128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19240277-T-C

22946153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19240302-T-C

22955506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243191-G-A

22955506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243191-G-C

22955506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243191-G-T

22955521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243206-G-T

22955655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243318-G-A

22955655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243318-G-T

22955739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243382-G-T

http://identifiers.org/hco/10/GRCh38#22955743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19243386-C-A

22955743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243386-C-T

22955758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243399-A-G

22955778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243423-G-A

22955778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243423-G-T

22955780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19243425-G-A

22955802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19243447-G-A

http://identifiers.org/hco/10/GRCh38#22956072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19243696-C-A

22959113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 19248803-T-C

22959148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19248838-C-T

22959321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19249019-G-A

22959764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19250091-T-G

22960226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19251169-A-G

22960227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19251170-G-C

22960795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19252040-A-G

22960798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19252043-A-G

22961154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19252337-T-A

22961154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19252337-T-C

22961395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19252964-G-A

22961454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253017-T-C

22961462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253025-G-A

22961607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253147-G-A

22961607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253147-G-C

22961607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253147-G-T

http://identifiers.org/hco/10/GRCh38#22961648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19253183-A-C

22961726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253249-T-C

22961817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253322-G-A

22961817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253322-G-T

22961837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253342-A-G

22961837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253342-A-T

22961880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19253394-G-A

22961971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19253485-T-C

http://identifiers.org/hco/10/GRCh38#22962023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19253537-C-A

22962023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19253537-C-T

22962069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19253583-A-G

http://identifiers.org/hco/10/GRCh38#22962094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19253603-C-A

22962217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253698-G-A

22962217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253698-G-T

22962227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253706-G-A

22962227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253706-G-T

22962346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253796-C-T

22962428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19253884-T-C

22967590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19257550-T-C

22967662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19257635-C-T

22967691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19257672-G-A

22967891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19257860-G-A

22968127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19258181-G-A

22968146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19258194-G-A

22968146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19258194-G-C

http://identifiers.org/hco/10/GRCh38#22968217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19258261-C-A

22968217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19258261-C-T

22968292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19258646-G-A

22968309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19258670-T-C

http://identifiers.org/hco/10/GRCh38#22968392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19258753-A-C

http://identifiers.org/hco/10/GRCh38#22968498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19258859-C-A

22968498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19258859-C-T

22969229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19259272-T-C

22969297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19259343-T-A

22969742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19260338-G-T

22974194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19266576-G-T

22974211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19266593-A-T

22974212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19266594-A-G

22974387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19266739-A-G

22976211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19269036-T-C

22976365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19269162-T-C

22976575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19269358-A-T

22976774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19269533-T-G

22976948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19269695-C-G

22976985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19269728-G-A

22978638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19271058-A-G

22979226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19271578-A-T

22979290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19271642-C-T

22979587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19271991-G-A

22979852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19272378-G-C

22979857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19272383-G-A

22980115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19272602-A-T

22980138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19272624-A-G

22980779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19273374-T-C

22980825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19273423-A-G

22980852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19273439-C-T

22981222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19273784-T-C

22981530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274076-G-A

22981530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274076-G-T

22981711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274951-A-T

22981712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274952-G-C

22981712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274952-G-T

22981737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274983-G-A

22981737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19274983-G-C

22983948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19276136-G-A

22984047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19276236-T-G

22984100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19276285-T-A

22984191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19276378-C-T

22984710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19277531-C-T

22984722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19277543-C-T

22984735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19277555-C-T

22986782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19279069-G-A

22987047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19279300-T-A

22987579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19279807-C-T

22987614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19279841-A-G

22987813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19280028-T-C

22987853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19280068-G-T

22989343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19281539-A-G

22989611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19281750-G-T

22989653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19281814-T-C

22989670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19281831-C-T

22989710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282042-T-A

22989710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282042-T-G

22989798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282128-T-C

22990200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282552-C-T

22990262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282620-C-G

22990323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282682-G-A

22990326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282685-T-A

22990436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282792-T-C

22990504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19282821-T-C

22990880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283188-T-C

22991026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283291-T-C

22991051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283316-T-C

22991078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283367-T-G

22991177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283476-C-G

22991271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283596-A-G

22991422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283807-T-C

22991442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19283817-G-T

22991603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284084-G-A

22991657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284152-G-A

22991683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284179-C-T

22991697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284199-G-A

http://identifiers.org/hco/10/GRCh38#22991708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19284210-A-C

22991876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284316-T-C

22991965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284401-C-T

22991980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284416-T-C

22991980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284416-T-G

22992555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284883-T-C

22992685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19284968-G-A

http://identifiers.org/hco/10/GRCh38#22992806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19285172-A-C

22992850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19285227-C-T

22993064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19285442-A-G

22993064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19285442-A-T

22993345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19285707-T-C

22995183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19288293-T-A

22995183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19288293-T-C

22995183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19288293-T-G

22995554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19288574-G-C

22995696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19288703-G-A

22997024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19289717-G-T

22997941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19290547-A-G

22997958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19290564-T-C

22998033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19290621-T-C

22998215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19290765-A-G

22998285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19290835-A-T

22998379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19290929-C-T

23000404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19291893-A-G

23000461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19291962-A-T

23000513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292012-T-C

23000550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292049-T-C

23000551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292050-G-T

23000899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292546-A-G

23000902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292549-C-T

23000960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292603-G-C

23001388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19292984-T-G

23001489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19293068-C-T

23001822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19293370-T-G

23001910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19293627-T-A

23001910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19293627-T-C

23002108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19293815-G-A

http://identifiers.org/hco/10/GRCh38#23002112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19293819-C-A

23002582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19294242-C-T

23003138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19297649-A-G

23003138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19297649-A-T

23003189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19297698-G-A

23003189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19297698-G-T

23003237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19297779-T-C

23003238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19297780-A-T

http://identifiers.org/hco/10/GRCh38#23003354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19297901-C-A

23003354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19297901-C-T

23006772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19300080-G-T

23006776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19300084-G-T

23006937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 19300253-A-G

23006994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300309-A-G

23007001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300316-G-A

23007001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300316-G-C

23007079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300386-T-C

23007121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300423-T-C

23007246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300503-C-G

23007246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19300503-C-T

23008142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301014-T-C

23008224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301085-T-C

23008262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301120-G-A

http://identifiers.org/hco/10/GRCh38#23008356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#19301217-C-A

23008356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 19301217-C-G

23008356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19301217-C-T

23008380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301241-A-G

23008451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301324-G-A

23008451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301324-G-T

http://identifiers.org/hco/10/GRCh38#23008492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19301362-A-C

23008492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301362-A-G

23008492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301362-A-T

http://identifiers.org/hco/10/GRCh38#23008811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19301599-C-A

23008811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19301599-C-T

23008840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19301631-G-A

23008841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19301632-G-T

23009011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301818-T-A

23009011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19301818-T-C

http://identifiers.org/hco/10/GRCh38#23030470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19305156-C-A

23030470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19305156-C-T

23030654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305341-G-C

http://identifiers.org/hco/10/GRCh38#23030922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19305645-C-A

23030922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19305645-C-T

http://identifiers.org/hco/10/GRCh38#23030950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19305675-C-A

23030950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19305675-C-T

23030959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 19305681-T-A

http://identifiers.org/hco/10/GRCh38#23031027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19305758-C-A

23031028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305759-A-G

http://identifiers.org/hco/10/GRCh38#23031039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19305770-C-A

23031047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305778-T-G

23031063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305794-A-G

23031121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305855-G-A

23031121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305855-G-C

23031121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305855-G-T

23031122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305856-G-T

23031130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305864-G-A

23031130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 19305864-G-T

23031289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19306032-G-A

23031289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19306032-G-T

23031469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19306201-G-A

23031485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19306211-C-G

http://identifiers.org/hco/10/GRCh38#23032238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19307775-C-A

http://identifiers.org/hco/10/GRCh38#23032248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19307781-C-A

23032759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19308517-G-T

23032814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19308563-G-A

23032830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19308579-G-T

23033137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19308880-A-G

23036842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19314323-G-A

23036894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19314367-C-T

http://identifiers.org/hco/10/GRCh38#23037036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19314515-A-C

http://identifiers.org/hco/10/GRCh38#23037221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19314677-C-A

23037221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 19314677-C-T

23037361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 19314819-G-A

23037527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19314983-A-G

http://identifiers.org/hco/10/GRCh38#23037563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#19315008-C-A

23037563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19315008-C-G

23037642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19315085-T-C

23037643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19315086-G-A

23038307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19316112-T-A

23038307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19316112-T-C

23038382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19316145-A-G

23038431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19316192-T-G

23038432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30964
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 19316193-G-C