42897008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26609165-G-A

42897008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26609165-G-C

42897052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26609126-G-A

42897052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26609126-G-T

http://identifiers.org/hco/8/GRCh38#42897245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#26608933-C-A

42897245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26608933-C-T

42897267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26608911-G-A

42897267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26608911-G-T

http://identifiers.org/hco/8/GRCh38#42897281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26608896-C-A

42897281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608896-C-T

http://identifiers.org/hco/8/GRCh38#42897320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26608803-C-A

42897320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26608803-C-G

42897320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26608803-C-T

http://identifiers.org/hco/8/GRCh38#42897431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26608675-C-A

42897431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26608675-C-T

42897508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26608563-C-T

42897654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26608394-G-A

42898292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26607559-G-C

42898424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26607431-C-T

42900367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26605660-G-A

42900573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26604920-C-T

42900787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26604822-T-C

42900959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26604663-A-G

42901207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26604388-G-A

42901644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26604139-T-C

42901653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26604129-G-A

42903565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26602846-C-T

42903571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26602829-C-T

42903621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26602774-A-G

42903638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26602760-C-T

http://identifiers.org/hco/8/GRCh38#42903641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26602757-C-A

42903664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26602734-T-C

42904284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26602155-T-C

http://identifiers.org/hco/8/GRCh38#42904661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26602103-A-C

42904837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601926-T-G

42904887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601876-T-C

42904960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601816-T-C

42905029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601693-T-C

42905046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601663-A-G

42905205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601508-A-G

42905272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601450-G-T

42905510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26601118-T-G

42905660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600974-T-C

http://identifiers.org/hco/8/GRCh38#42906101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26600908-A-C

42906101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600908-A-T

http://identifiers.org/hco/8/GRCh38#42906133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26600871-C-A

42906133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600871-C-T

http://identifiers.org/hco/8/GRCh38#42906135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26600869-A-C

42906135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600869-A-G

http://identifiers.org/hco/8/GRCh38#42906144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26600860-C-A

42906144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600860-C-G

42906144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600860-C-T

http://identifiers.org/hco/8/GRCh38#42906176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26600844-C-A

42906176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 26600844-C-T

42906192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600828-A-G

42906194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600826-G-A

42906208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26600812-C-G

42906208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26600812-C-T

42906209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600811-G-A

42906209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600811-G-C

42906209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600811-G-T

42906212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600808-G-A

42906215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26600805-G-A

http://identifiers.org/hco/8/GRCh38#42906268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26600752-A-C

42906296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600724-G-A

42906296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26600724-G-T

42907149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26599005-A-G

42907485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598663-G-A

42907499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26598649-G-C

42920051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26590529-T-C

42921852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26588250-A-G

42922209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26587920-C-T

42925427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26585969-T-G

42925484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26585912-A-G

42925540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26585872-T-C

42925563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26585850-T-C

42925672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26585735-G-A

42925731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26585680-G-A

42925731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26585680-G-C

42925897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26585511-T-C

42930064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583790-A-G

42930188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583665-T-A

42930188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583665-T-C

http://identifiers.org/hco/8/GRCh38#42930299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26583565-C-A

42930494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583324-A-G

http://identifiers.org/hco/8/GRCh38#42930720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26583051-C-A

42930720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26583051-C-T

42932412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26580984-A-G

http://identifiers.org/hco/8/GRCh38#42932501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26580893-C-A

42932673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26580680-A-G

42941620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578921-T-A

42941633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578907-G-C

42942791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578716-G-T

42942897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578618-C-T

42942910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578605-A-G

42942911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578604-T-C

42943097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578430-G-A

42943288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578243-T-A

42943288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578243-T-C

42943297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578234-T-C

http://identifiers.org/hco/8/GRCh38#42943370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26578161-C-A

42943370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26578161-C-G

42943370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26578161-C-T

http://identifiers.org/hco/8/GRCh38#42943400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26578131-C-A

42943400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26578131-C-T

42943484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578072-G-A

http://identifiers.org/hco/8/GRCh38#42943560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26578005-C-A

42943560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26578005-C-T

42943582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26577991-G-T

42943641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26577932-C-T

42945869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26576603-G-C

42946285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575963-G-A

42946446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575816-C-T

42946459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575794-G-C

42946782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575481-T-C

42946838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26575430-G-C

42947694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574780-T-C

42948048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574485-T-A

42948048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574485-T-G

42948211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26574072-T-G

42948347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573937-G-A

42949966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26573144-T-G

42950181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26572942-A-T

42950194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26572908-C-T

42950330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26572665-G-A

42950330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26572665-G-T

42950544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26572449-T-A

42955529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568945-T-C

42955540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26568934-A-G

42956384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26565263-C-T

42956476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26565152-T-C

42956936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26565107-C-T

42956971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26565068-G-A

42956971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26565068-G-T

http://identifiers.org/hco/8/GRCh38#42956973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26565066-A-C

42956973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26565066-A-G

42957187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564870-A-G

42957239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564818-T-C

http://identifiers.org/hco/8/GRCh38#42957278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26564777-C-A

http://identifiers.org/hco/8/GRCh38#42958046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26564389-A-C

42958123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26564318-C-T

42958423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563963-A-G

http://identifiers.org/hco/8/GRCh38#42959090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26563840-C-A

42959090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563840-C-G

42959200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563747-T-C

42959212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563735-T-C

http://identifiers.org/hco/8/GRCh38#42959312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26563628-C-A

42959312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 26563628-C-T

42959327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563610-T-C

http://identifiers.org/hco/8/GRCh38#42959329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26563608-C-A

42959329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26563608-C-G

42963637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562978-A-G

42963970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562777-G-A

http://identifiers.org/hco/8/GRCh38#42963991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26562755-A-C

42964006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562740-G-A

http://identifiers.org/hco/8/GRCh38#42964035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26562712-A-C

42964035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562712-A-G

42964259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26562474-T-C

42966531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26561166-T-C

42967937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560379-A-G

http://identifiers.org/hco/8/GRCh38#42967960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26560347-C-A

42967960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560347-C-G

42967967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560340-A-T

42967973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560334-G-T

http://identifiers.org/hco/8/GRCh38#42967993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26560319-A-C

42967999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560313-C-T

http://identifiers.org/hco/8/GRCh38#42968140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26560174-A-C

42968140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26560174-A-G

42968236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560074-G-C

http://identifiers.org/hco/8/GRCh38#42968259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26560051-C-A

http://identifiers.org/hco/8/GRCh38#42968269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26560041-A-C

42968269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560041-A-G

42968272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26560038-T-C

42972888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559186-A-G

42973113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559012-G-A

42973113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26559012-G-C

42973167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558958-T-C

42973197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558924-G-T

42973237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558806-T-A

42973237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558806-T-C

42973364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26558620-A-G

42973414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558572-T-G

42973460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558529-T-A

42973460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558529-T-C

42973617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558402-T-C

42973624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558395-A-G

42973779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558270-A-G

42973921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558138-A-G

42973985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558066-G-A

42973985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558066-G-T

42973990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558061-A-T

42974018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558033-T-C

42974018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26558033-T-G

42974238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26557839-T-A

http://identifiers.org/hco/8/GRCh38#42974291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26557804-C-A

42974291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26557804-C-T

42974324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26557783-T-C

http://identifiers.org/hco/8/GRCh38#42974343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26557763-C-A

42974343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26557763-C-T

42974349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26557757-T-C

http://identifiers.org/hco/8/GRCh38#42980399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26556427-C-A

42981647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26556210-G-C

42981653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26556204-G-A

42982311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551893-C-T

http://identifiers.org/hco/8/GRCh38#42982312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26551892-C-A

42982358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551842-G-A

42982548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551560-G-A

42982548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551560-G-T

42982561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551547-T-C

42982590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551503-T-G

http://identifiers.org/hco/8/GRCh38#42982636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26551463-C-A

42982636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26551463-C-T

42982715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551386-T-C

42982840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26551266-A-G

42986591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26549453-T-C

42986767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26549294-C-T

42987493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26548622-G-A

42988231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26546104-A-T

42997444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26538463-T-C

42997458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26538449-G-A

42997533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26538382-G-A

42997679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26538236-A-G

42997769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26537969-C-T

http://identifiers.org/hco/8/GRCh38#42997868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26537902-C-A

42998001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26537845-A-G

42998216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537647-T-C

42998216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537647-T-G

42998235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537629-A-G

42998236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537628-G-A

42998635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537303-G-A

42998736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537211-T-C

42998766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26537182-T-C

42999058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26536770-G-A

42999382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26536507-T-C

42999524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26536366-C-G

http://identifiers.org/hco/8/GRCh38#43000225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26535983-C-A

43000225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535983-C-T

43000331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535870-T-A

43000331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535870-T-C

43000365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535839-A-G

http://identifiers.org/hco/8/GRCh38#43000387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26535817-A-C

43000387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535817-A-G

43000429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535773-T-G

43000692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535574-G-A

43000692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535574-G-T

http://identifiers.org/hco/8/GRCh38#43000719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26535542-C-A

43000742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26535520-A-G

43000957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26535323-A-G

43000965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26535314-T-C

43000971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26535308-G-A

43000971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26535308-G-T

43001288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26535008-A-G

43001452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534855-C-T

43001563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534744-C-T

43001565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534741-C-T

43001597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534714-G-A

http://identifiers.org/hco/8/GRCh38#43001837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26534531-C-A

43001964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534441-A-G

http://identifiers.org/hco/8/GRCh38#43002026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26534381-C-A

43002214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534200-G-T

43002245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534169-A-G

43002270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26534146-T-A

43002579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26533752-G-A

43003174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26532834-C-T

43003460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26532583-T-C

43003515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26532531-T-G

43003749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26532298-G-C

43006884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26530791-C-G

43006932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26530736-G-A

43007000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26530672-C-G

43007000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26530672-C-T

43007009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26530663-T-G

43007817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26529813-T-C

http://identifiers.org/hco/8/GRCh38#43007905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26529719-C-A

43007970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26529666-T-A

43007970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26529666-T-C

43007984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26529652-G-A

43007984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26529652-G-T

43010419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26528035-T-C

43010647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26527831-G-C

43013038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26525277-T-C

http://identifiers.org/hco/8/GRCh38#43013056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26525258-C-A

43013056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26525258-C-T

43013173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26525143-A-T

43013258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26525084-T-A

43013445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26524913-A-T

43013551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26524812-G-A

43013551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26524812-G-T

43015272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26524202-C-T

43015681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26523820-A-G

http://identifiers.org/hco/8/GRCh38#43017582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26522801-A-C

43017881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26522528-A-G

43017890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26522519-T-G

http://identifiers.org/hco/8/GRCh38#43017930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26522480-A-C

43017943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26522467-A-G

43017962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26522451-G-A

43018105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26522313-T-C

43018202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: intron variant
orthologous variants: 26522216-A-T

43018475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense variant
orthologous variants: 26521939-G-A

43018475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense variant
orthologous variants: 26521939-G-C

43018475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: missense variant
orthologous variants: 26521939-G-T

http://identifiers.org/hco/8/GRCh38#43018649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26521782-C-A

43018649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26521782-C-T

43018921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26521509-G-A

http://identifiers.org/hco/8/GRCh38#43018938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26521492-C-A

http://identifiers.org/hco/8/GRCh38#43018971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26521459-C-A

43018979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26521446-C-T

43018989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26521436-T-C

http://identifiers.org/hco/8/GRCh38#43019004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26521422-C-A

43019004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26521422-C-G

43019442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26521060-C-G

http://identifiers.org/hco/8/GRCh38#43019539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26520966-C-A

43019724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26520799-G-A

43019724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26520799-G-T

http://identifiers.org/hco/8/GRCh38#43019769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26520753-C-A

43019981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26520537-T-A

http://identifiers.org/hco/8/GRCh38#43021113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26519594-A-C

43021113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519594-A-G

http://identifiers.org/hco/8/GRCh38#43021124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26519583-A-C

http://identifiers.org/hco/8/GRCh38#43021133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26519574-A-C

43021137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519572-T-A

43021137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519572-T-C

43021137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519572-T-G

http://identifiers.org/hco/8/GRCh38#43021145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26519564-C-A

43021162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519548-T-C

43022108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519233-T-A

43022108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519233-T-C

43022108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519233-T-G

43022123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519218-G-T

http://identifiers.org/hco/8/GRCh38#43022210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26519134-C-A

43022210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519134-C-T

43022241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519122-A-G

http://identifiers.org/hco/8/GRCh38#43022315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26519090-C-A

43022315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519090-C-T

43022320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26519085-C-T

http://identifiers.org/hco/8/GRCh38#43023833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26517742-C-A

43023833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517742-C-T

http://identifiers.org/hco/8/GRCh38#43023961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26517626-C-A

43023994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517592-T-C

43024017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517562-G-T

43024035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517544-A-G

43024037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517542-G-A

43024055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517528-A-G

http://identifiers.org/hco/8/GRCh38#43024073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26517510-C-A

43024073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517510-C-T

43024275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517290-G-T

43024279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517286-T-C

43024329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26517239-A-G

43024375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516804-G-T

43024382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516797-A-G

43024406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516773-A-G

43024469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516686-C-T

http://identifiers.org/hco/8/GRCh38#43024481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26516674-C-A

43024493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516662-C-T

http://identifiers.org/hco/8/GRCh38#43024782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26516405-C-A

http://identifiers.org/hco/8/GRCh38#43024829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26516344-C-A

43025061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516129-T-C

43025118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26516076-A-G

43025198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515968-A-G

43025202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515964-A-G

43025332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515779-A-G

43025634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515508-T-C

43025761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515377-C-T

43025865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515275-A-G

43025935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515183-G-A

43026029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515087-T-C

43026029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515087-T-G

43026052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26515065-A-G

43026193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514961-T-C

http://identifiers.org/hco/8/GRCh38#43026202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26514950-C-A

43026402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514790-T-C

http://identifiers.org/hco/8/GRCh38#43026449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26514748-C-A

http://identifiers.org/hco/8/GRCh38#43026681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26514558-C-A

43026681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514558-C-T

43026682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514557-C-G

43026693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514541-C-T

43026817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514416-G-C

http://identifiers.org/hco/8/GRCh38#43027268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26514304-C-A

43027268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514304-C-T

43027300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514275-A-G

43027331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26514246-A-G

43027433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: 26514157-G-A

http://identifiers.org/hco/8/GRCh38#43028876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#26512422-C-A

43028917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: 26512381-T-C

43028980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: 26512320-C-G

43029015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: 26512285-T-C

43029533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: 26512084-A-G

43029572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23576
most severe consequence: 3 prime UTR variant
orthologous variants: 26512046-A-G