233475789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87873109-A-G

233475808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87873115-T-A

233477219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874134-G-A

233477219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874134-G-T

233477235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874149-T-C

233477243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874157-C-G

233477243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874157-C-T

http://identifiers.org/hco/2/GRCh38#233477318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87874240-C-A

233477318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874240-C-G

233477318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874240-C-T

233477363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 87874287-A-T

233477454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87874380-T-A

233477496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87874422-C-T

http://identifiers.org/hco/2/GRCh38#233481186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87876207-C-A

233481186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87876207-C-T

233481227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87876248-T-C

233485514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87877641-G-T

233485645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87877768-T-A

233485908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87878022-G-A

233485921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87878035-G-A

http://identifiers.org/hco/2/GRCh38#233485965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87878079-C-A

233485965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87878079-C-T

233485972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87878086-T-C

http://identifiers.org/hco/2/GRCh38#233486028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87878127-C-A

233486028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87878127-C-G

233486028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87878127-C-T

http://identifiers.org/hco/2/GRCh38#233486043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87878142-C-A

233486043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87878142-C-T

233486068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87878165-G-A

233486068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87878165-G-T

http://identifiers.org/hco/2/GRCh38#233487592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87878739-C-A

233487889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87878995-G-A

233487889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87878995-G-T

233488003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87879078-G-A

233488003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 87879078-G-T

233488108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87879238-T-A

233488108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87879238-T-C

233488118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87879259-G-T

http://identifiers.org/hco/2/GRCh38#233488371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87879487-C-A

http://identifiers.org/hco/2/GRCh38#233488430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87879547-C-A

233488430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87879547-C-T

http://identifiers.org/hco/2/GRCh38#233489349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87880048-C-A

233490634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87881345-G-A

233490767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87881444-T-C

233491169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 87881875-G-A

http://identifiers.org/hco/2/GRCh38#233491218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87881924-C-A

233491280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87881985-G-C

233491280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87881985-G-T

233491343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882033-T-C

233491355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882050-T-C

233491359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882054-A-T

233491401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882095-G-T

233491433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882127-T-A

233491433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882127-T-C

233491434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882128-G-A

233491434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882128-G-T

233491504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87882191-T-C

http://identifiers.org/hco/2/GRCh38#233491514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87882201-A-C

233492562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87883415-C-G

http://identifiers.org/hco/2/GRCh38#233492982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87883750-C-A

233493021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87883795-G-T

233493046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87883829-G-T

233493534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87885039-G-A

233493567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87885072-T-C

233496495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87887025-G-A

http://identifiers.org/hco/2/GRCh38#233496562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87887325-A-C

http://identifiers.org/hco/2/GRCh38#233496625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87887382-C-A

233496676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87887442-T-C

233496824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87887577-T-C

http://identifiers.org/hco/2/GRCh38#233496842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87887595-C-A

233496842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87887595-C-T

233496902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87887651-A-G

233497264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87887994-C-T

233497730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87889202-C-T

233498462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87889828-T-C

233498462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87889828-T-G

233498530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87890128-G-A

233498690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87892501-T-A

233498745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87892552-G-A

233498745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87892552-G-T

233498785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87892591-C-G

http://identifiers.org/hco/2/GRCh38#233498798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87892604-C-A

http://identifiers.org/hco/2/GRCh38#233498920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87892704-C-A

233498920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87892704-C-T

233499724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87892875-C-T

233499866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87893015-G-C

233499866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87893015-G-T

233509088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87894219-G-A

233509129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 87894259-T-C

233509186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894316-A-G

233509186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894316-A-T

233509376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894471-C-T

233509911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894802-G-A

233509911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894802-G-C

233509911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894802-G-T

233509997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894889-G-A

233509997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87894889-G-T

233511658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87895187-T-C

233511747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87895270-A-G

233511747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87895270-A-T

233511748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87895271-T-C

233511748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87895271-T-G

http://identifiers.org/hco/2/GRCh38#233512167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87895749-C-A

233512167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895749-C-G

233512167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895749-C-T

233512218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895800-T-C

http://identifiers.org/hco/2/GRCh38#233512235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87895817-C-A

233512295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895869-T-C

233512414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895969-T-G

233512429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895980-G-A

233512429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87895980-G-T

233512473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87896022-A-G

233512496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87896045-A-G

233512496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87896045-A-T

http://identifiers.org/hco/2/GRCh38#233512804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87896438-C-A

233512804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87896438-C-G

http://identifiers.org/hco/2/GRCh38#233512858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87896523-C-A

233512858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87896523-C-T

233513012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87896648-A-T

233513869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87897628-G-A

233513870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87897629-T-C

233514078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87897832-G-C

233514385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898195-G-A

233514490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898298-A-G

http://identifiers.org/hco/2/GRCh38#233514662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87898467-C-A

233514796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898601-C-T

233515059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898834-T-C

233515107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898866-C-T

233515108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898867-G-A

233515108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87898867-G-T

233515454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87899192-A-G

233515525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87899296-G-A

233518528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87900881-C-T

233518630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87900970-T-C

233518971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87901249-C-T

http://identifiers.org/hco/2/GRCh38#233519382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87901591-C-A

233519382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87901591-C-G

233519432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87901635-T-G

233519779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87901959-G-C

233519794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87901965-T-C

233520143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87902277-G-A

233520301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87902426-T-A

233520324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87902446-T-A

233520324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87902446-T-C

233520718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87903301-G-A

233521045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87903584-T-C

233521235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87903778-A-T

233521339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87903993-C-T

233521575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87904218-T-G

233522324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87905313-A-G

233523235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87906101-C-G

233523235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87906101-C-T

233523288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87906154-A-G

233523288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87906154-A-T

233523480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87906346-C-T

233523530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87906396-T-G

233523616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87906493-T-C

http://identifiers.org/hco/2/GRCh38#233523832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87906678-C-A

233523848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87906695-C-G

233523848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87906695-C-T

233523921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87906751-G-A

233524072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87906957-G-A

233524332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87907476-G-C

233524345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87907489-G-T

http://identifiers.org/hco/2/GRCh38#233524429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87907674-C-A

233524580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87907828-G-A

233524905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87908086-C-T

233525350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87908549-G-T

233525353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87908552-G-C

233525353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87908552-G-T

233525442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87908658-A-G

233525963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87909216-C-T

233526006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87909244-T-C

http://identifiers.org/hco/2/GRCh38#233527683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87910088-C-A

233527683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910088-C-T

233527975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910304-C-T

233528465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910473-G-A

233528501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910520-C-T

233528620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910612-A-G

233528695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910667-T-G

233528807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87910834-C-G

233528896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87911006-G-A

http://identifiers.org/hco/2/GRCh38#233529442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87911487-C-A

233529442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87911487-C-T

http://identifiers.org/hco/2/GRCh38#233529509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87911554-C-A

233529509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87911554-C-T

233529556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87911601-T-C

233533489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87913634-T-C

233533704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87913846-G-A

233533717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87913859-C-G

233533831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87914002-A-T

233533850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87914016-T-C

233533870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87914052-G-A

233540056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916003-T-A

233540056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916003-T-C

233540117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916044-T-A

233540117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916044-T-C

http://identifiers.org/hco/2/GRCh38#233540134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87916061-A-C

http://identifiers.org/hco/2/GRCh38#233540178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87916090-C-A

233540429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916354-C-T

http://identifiers.org/hco/2/GRCh38#233540548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87916494-C-A

233540548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916494-C-T

233540631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87916575-T-G

http://identifiers.org/hco/2/GRCh38#233542188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87917687-C-A

233542188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87917687-C-G

233542188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87917687-C-T

233542214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87917712-C-T

http://identifiers.org/hco/2/GRCh38#233542242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87917758-C-A

233542242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87917758-C-T

233542403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87917923-T-A

233542403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87917923-T-C

233542469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87917996-G-A

233542469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87917996-G-T

233542477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87918003-G-A

233542477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87918003-G-T

http://identifiers.org/hco/2/GRCh38#233546254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87921306-C-A

233546254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87921306-C-G

233546254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87921306-C-T

233546390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87921373-A-G

233546487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87921455-G-A

233546487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87921455-G-T

233548700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87921572-G-A

233548700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87921572-G-C

233549006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87921798-G-C

233549006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87921798-G-T

233549076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87921871-T-C

233549143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87921938-T-A

233549143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87921938-T-C

233549197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87921992-G-T

233549240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87922032-A-G

http://identifiers.org/hco/2/GRCh38#233551327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87923385-C-A

233551327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87923385-C-T

233551389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87923446-G-A

233551629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87924081-T-C

http://identifiers.org/hco/2/GRCh38#233554246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87925402-A-C

http://identifiers.org/hco/2/GRCh38#233554300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87925457-C-A

233554300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87925457-C-T

233554330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87925496-T-C

233554471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87925626-G-C

233554540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87925695-G-A

233554664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87925811-G-A

233554664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87925811-G-T

233554734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87925877-T-C

http://identifiers.org/hco/2/GRCh38#233556195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87926688-C-A

233556240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87926726-T-G

233556504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87926967-C-T

http://identifiers.org/hco/2/GRCh38#233556585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87927214-C-A

233556740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87927349-T-A

233556740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87927349-T-C

233556799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87927407-T-C

233556814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87927422-T-G

233556847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87927454-A-G

233557005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87927612-A-G

233557030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87927637-G-A

233557030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87927637-G-C

233557061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87927784-A-T

233557147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87927864-T-A

http://identifiers.org/hco/2/GRCh38#233557313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87928012-A-C

233557636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928285-G-C

233557636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928285-G-T

233557729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87928370-A-G

233557789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928427-T-C

233557818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928455-G-C

233557832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928469-G-A

233558119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928604-C-T

233558139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928624-G-A

233558181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928655-C-G

233558181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87928655-C-T

233558732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87929111-G-A

233559395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87929754-A-T

233559704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930044-T-A

233559704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930044-T-C

233559707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930047-G-T

http://identifiers.org/hco/2/GRCh38#233559994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87930305-C-A

233560068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930379-A-G

http://identifiers.org/hco/2/GRCh38#233560168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87930468-C-A

233560186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930486-C-G

233560605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930843-T-C

233560680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87930916-T-G

http://identifiers.org/hco/2/GRCh38#233560708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87930943-C-A

http://identifiers.org/hco/2/GRCh38#233560790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87931032-C-A

233560790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931032-C-G

http://identifiers.org/hco/2/GRCh38#233560848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87931093-C-A

233560848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931093-C-T

233560866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931097-G-T

233560869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931100-A-G

233560888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931119-G-A

http://identifiers.org/hco/2/GRCh38#233560951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87931180-C-A

233560951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931180-C-T

233561074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87931286-G-T

233561169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931978-G-A

233561169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931978-G-C

233561169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87931978-G-T

233562867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932099-A-G

233562992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932224-T-C

233563140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932541-C-T

http://identifiers.org/hco/2/GRCh38#233563314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87932714-C-A

233563314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932714-C-G

233563314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932714-C-T

233563491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932790-T-C

233563700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932945-C-G

233563700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87932945-C-T

233564389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934038-C-T

http://identifiers.org/hco/2/GRCh38#233564579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87934217-C-A

233564579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934217-C-T

233565176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934773-G-T

http://identifiers.org/hco/2/GRCh38#233565211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87934806-C-A

233565211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934806-C-T

233565252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934847-G-A

233565252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934847-G-C

233565252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934847-G-T

233565271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934865-T-C

233565271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934865-T-G

233565284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934878-G-A

233565284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934878-G-C

233565284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87934878-G-T

233565408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87934999-G-C

233565476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87935067-T-C

233565609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87935203-A-T

233565643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87935239-C-T

233565815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87935408-T-C

233566306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87935819-T-C

233566313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87935826-G-C

233566437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87935955-G-A

233566437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87935955-G-C

233566597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87936083-G-A

233566597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87936083-G-T

233566630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87936107-G-T

http://identifiers.org/hco/2/GRCh38#233566661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87936137-C-A

233566661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87936137-C-T

233566708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87936184-T-G

233566760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87936236-G-A

233566761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87936237-C-G

233566761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20069
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 87936237-C-T