http://identifiers.org/hco/5/GRCh38#123512342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#53995481-C-A

http://identifiers.org/hco/5/GRCh38#123512355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#53995494-A-C

123512355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995494-A-G

123512358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995497-G-A

123512358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995497-G-T

123512361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995500-C-G

123512361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995500-C-T

123512381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995513-T-A

123512381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995513-T-C

123512419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995550-G-A

123512427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995558-G-A

123512427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995558-G-T

123512473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995601-T-C

123512473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53995601-T-G

123513037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53995910-G-A

http://identifiers.org/hco/5/GRCh38#123513085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#53995933-A-C

123513371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53996087-C-T

123513489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53996193-T-G

123514131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53996785-C-G

http://identifiers.org/hco/5/GRCh38#123514326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#53997134-C-A

123514672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53997464-G-C

123515681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998457-A-G

123515706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998472-T-G

123515707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998473-T-C

123515708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998474-T-G

123515827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998576-C-T

123515891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998638-A-G

http://identifiers.org/hco/5/GRCh38#123515919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#53998666-A-C

123516049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998786-A-G

http://identifiers.org/hco/5/GRCh38#123516115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#53998851-A-C

123516124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53998864-C-T

123516349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999091-A-T

123517024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999756-T-C

123517076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999782-A-G

123517079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999785-A-G

123517297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53999989-T-C

123517522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54000212-G-A

123517683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54000351-C-G

123517683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54000351-C-T

123517700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54000368-T-G

123517702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54000370-G-A

123518485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54001368-G-A

123518485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54001368-G-C

123518806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54001647-G-A

123519616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54002065-T-C

http://identifiers.org/hco/5/GRCh38#123521044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54010917-A-C

123521526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54011339-C-T

123521632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54011447-A-G

123522869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54012230-C-G

123522869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54012230-C-T

123522921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54012283-A-T

http://identifiers.org/hco/5/GRCh38#123523529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54012949-C-A

123523529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54012949-C-T

123523928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54013685-T-C

123523954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54013693-A-G

123523969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54013710-C-T

http://identifiers.org/hco/5/GRCh38#123524097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54013831-A-C

123524097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54013831-A-G

123524295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014091-G-T

123524531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014299-A-G

123524555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014323-C-T

123524582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014341-C-G

123524690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014446-G-A

http://identifiers.org/hco/5/GRCh38#123524772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54014522-A-C

123524843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014593-T-A

123524843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014593-T-C

123524884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54014623-G-T

123528682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54015869-T-A

123530448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54019225-C-G

http://identifiers.org/hco/5/GRCh38#123530791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54019958-A-C

123530868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54020038-T-C

123531007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54020176-G-A

123531128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54020513-G-A

123531203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54020589-A-T

123531927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021204-G-A

123532057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54021320-G-C

123532625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54021834-A-G

123545370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54028561-T-C

123546674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54029571-T-A

123547255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54030031-T-A

123550073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54032945-A-G

123550343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033403-T-A

123550386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033443-G-C

123550461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033513-C-T

http://identifiers.org/hco/5/GRCh38#123550462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54033514-A-C

123550524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033559-G-A

http://identifiers.org/hco/5/GRCh38#123550735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54033755-A-C

123550807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033815-A-G

123550939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033952-A-G

123550958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54033970-T-C

123551390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54034396-A-G

123551810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54034754-A-T

http://identifiers.org/hco/5/GRCh38#123552143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: -A-C

123552370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: -T-C

123552393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/5/GRCh38#123552420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: -A-C

123552420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/5/GRCh38#123552898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54035708-C-A

123552905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54035715-T-C

123553015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54035820-T-C

123553015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54035820-T-G

http://identifiers.org/hco/5/GRCh38#123553021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54035826-A-C

123553021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54035826-A-G

123553021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54035826-A-T

123553022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54035827-T-C

123553294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036099-G-A

123553294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036099-G-T

123553519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036305-A-G

123553540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036328-C-T

123553996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036783-A-G

123554168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54036956-C-G

123554777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54038087-C-T

123554973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54038242-C-T

123555041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54038329-C-G

123555151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54038487-A-G

123555490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54038786-A-G

123557429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54039603-A-G

http://identifiers.org/hco/5/GRCh38#123557599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54039773-A-C

http://identifiers.org/hco/5/GRCh38#123558039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54040443-C-A

123558479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54040893-C-T

123558519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54040928-T-G

http://identifiers.org/hco/5/GRCh38#123558567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54041196-A-C

123563627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54045130-G-A

123563711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54045195-C-G

123570068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54047943-G-A

http://identifiers.org/hco/5/GRCh38#123570250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54048105-A-C

123570250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54048105-A-G

123570381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54048141-T-G

123570857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54048385-A-G

123572553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54049258-G-A

123573029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54049756-C-T

123573249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54049892-T-G

123573374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54050028-A-G

123573569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54050218-T-A

123573577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54050226-A-G

123574423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54050988-A-G

123574557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54051115-T-C

123575221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54051363-T-C

123575268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54051403-A-G

http://identifiers.org/hco/5/GRCh38#123575289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54051435-A-C

123575498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54051638-T-C

123575693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54051838-A-G

123575809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: synonymous variant
orthologous variants: 54051951-A-G

123576036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052178-A-G

123576066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052208-T-A

123576080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052222-C-T

123576099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052239-G-C

123576099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052239-G-T

http://identifiers.org/hco/5/GRCh38#123576303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54052409-A-C

123576303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052409-A-G

123576598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052657-C-G

123576598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052657-C-T

123576803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54052916-G-A

123576943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54053171-C-T

123577061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54053286-A-T

123577119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54053339-A-G

123577673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54053770-A-G

123578794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54053992-G-T

123579424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54054522-G-T

123579519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54054590-C-T

123579662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54054735-T-C

123581738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54056754-G-T

123581940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54057147-G-A

123582391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54057540-T-C

123582401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54057550-A-G

123582686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54057796-C-T

http://identifiers.org/hco/5/GRCh38#123582701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54057811-C-A

123582950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54058056-G-C

123583109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54058210-G-A

123587720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54062862-G-A

http://identifiers.org/hco/5/GRCh38#123587738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54062879-A-C

123587939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063033-G-C

123587939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063033-G-T

123588069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 54063142-A-G

123588252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063275-T-G

123588529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063453-G-A

123588529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063453-G-T

http://identifiers.org/hco/5/GRCh38#123588655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54063592-C-A

123588655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063592-C-G

123588655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063592-C-T

123588686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063623-T-C

123588824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063731-A-G

123588925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063803-G-T

123589013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063880-A-G

123589085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54063950-C-T

123589337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54064309-T-C

123589597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54064565-G-A

123589641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54064605-G-A

123589815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54064730-C-T

123590239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065145-C-T

123590398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065251-T-A

123590398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065251-T-C

http://identifiers.org/hco/5/GRCh38#123590447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54065300-A-C

123590447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: synonymous variant
orthologous variants: 54065300-A-G

http://identifiers.org/hco/5/GRCh38#123590590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54065449-C-A

123590590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065449-C-G

123590590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065449-C-T

123590665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065509-T-C

123590677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065521-T-A

123590677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065521-T-C

http://identifiers.org/hco/5/GRCh38#123590706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54065548-C-A

123590706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065548-C-T

123590909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065772-T-A

123590909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54065772-T-C

123591241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54066443-T-G

123591482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54066688-G-A

123591482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54066688-G-T

123591495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54066743-G-A

123591495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54066743-G-T

123591767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54066955-A-G

123591865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54067042-C-G

123592361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54067551-A-G

123592383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54067590-G-A

123592555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54067729-C-T

123592604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54067768-A-G

123592992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068045-T-G

123593249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068211-A-G

http://identifiers.org/hco/5/GRCh38#123593658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54068581-A-C

123593658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068581-A-G

123593732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068638-T-C

123593898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068817-G-A

123593904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068823-C-T

123593905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54068824-A-G

http://identifiers.org/hco/5/GRCh38#123594250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54069100-C-A

123594299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54069147-T-A

123594348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54069196-G-T

123594501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54069351-A-G

123594742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54069632-G-A

123595059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 54069945-T-C

123595233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54070115-T-C

123595369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54070246-A-G

123595675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54070487-T-C

123595729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54070525-T-C

123595804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54070598-G-A

123595829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54070612-A-G

123596469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54071176-C-T

123596844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54071504-A-G

123596927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54071613-T-C

123597764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54072755-A-T

123598108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54073057-T-C

123598464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54073355-G-A

123598923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54077455-G-A

123599052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54077582-C-T

123599506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54077968-G-T

123599744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54078215-G-C

123599889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54078360-A-G

123601091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54079230-C-G

123602965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54079481-T-C

123603038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54079552-C-G

123603256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54079760-T-C

123603256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54079760-T-G

123603566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54080057-A-G

123603658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54080296-A-G

123604120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54080719-T-G

123604129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54080728-A-G

123604243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54080805-A-G

123604291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54080854-A-G

123604582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081006-G-A

123604598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081022-A-G

123604622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081046-T-A

http://identifiers.org/hco/5/GRCh38#123604649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54081048-C-A

123604649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081048-C-G

123604649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081048-C-T

123604684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081077-G-A

123604684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081077-G-T

http://identifiers.org/hco/5/GRCh38#123604689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54081082-C-A

123604689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081082-C-T

http://identifiers.org/hco/5/GRCh38#123604756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54081152-A-C

123604756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: synonymous variant
orthologous variants: 54081152-A-G

123604834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081230-T-C

123604851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081247-T-A

123604861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081257-T-A

123604947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081335-A-G

123605127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081506-C-T

123605202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081580-T-C

123605232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081610-G-T

123605243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081619-G-A

123605243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081619-G-T

123605245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081621-A-G

http://identifiers.org/hco/5/GRCh38#123605446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54081821-C-A

123605446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081821-C-G

123605581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081951-A-G

123605583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54081953-A-G

123605862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54082201-T-A

123606540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54082757-G-A

http://identifiers.org/hco/5/GRCh38#123606626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54082840-C-A

123610290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083418-G-C

123610371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083508-A-G

123610372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083509-C-G

123610372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083509-C-T

123610418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083556-A-G

123610433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083572-T-C

123610490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083622-G-T

123610554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083710-T-A

123610575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54083731-A-G

123610943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54084203-G-C

http://identifiers.org/hco/5/GRCh38#123610970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54084229-C-A

123614020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54085967-C-G

123614048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54085991-G-C

123614172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54086151-T-C

123614187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: 54086161-C-T

http://identifiers.org/hco/5/GRCh38#123614306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54086282-C-A

123615058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087009-T-A

123615058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087009-T-C

123615176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087111-T-C

123615477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087406-T-C

123615568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087498-A-G

123615688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087606-G-T

123615954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087864-G-T

123616026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087935-T-C

123616059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54087968-G-T

123616330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088207-G-A

123616330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088207-G-T

123616548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088422-A-G

123616799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088675-T-C

123616820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088696-C-T

123616874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088749-G-T

123616891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088766-A-G

http://identifiers.org/hco/5/GRCh38#123616999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#54088869-C-A

123616999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2456
most severe consequence: 3 prime UTR variant
orthologous variants: 54088869-C-T