40621083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120753368-T-C

40621335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120753130-G-T

40621369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120753094-A-G

http://identifiers.org/hco/1/GRCh38#40622016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120752583-C-A

40622031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120752568-G-A

40622031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120752568-G-T

40622317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120752322-T-C

40622604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120752031-A-G

40622738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751906-G-T

40622750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751894-G-A

40622750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751894-G-T

40622781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751863-C-T

40622810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751834-G-A

40622884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751824-G-A

40622884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751824-G-C

40622884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751824-G-T

40622964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751744-G-T

40623027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751665-T-A

40623035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751657-T-G

40623053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751638-G-A

http://identifiers.org/hco/1/GRCh38#40623208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120751489-C-A

40623208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751489-C-T

40623292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751413-C-T

40623326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751381-G-T

http://identifiers.org/hco/1/GRCh38#40623445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120751251-C-A

40623445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751251-C-T

40623495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751202-A-T

40623541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751158-T-C

40623579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751126-G-A

40623579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751126-G-T

40623628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751103-G-A

40623628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751103-G-T

40623629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751102-G-A

40623629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751102-G-T

40623637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751095-T-A

40623637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751095-T-C

40623645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751087-T-A

40623645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120751087-T-C

http://identifiers.org/hco/1/GRCh38#40623701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120751030-A-C

http://identifiers.org/hco/1/GRCh38#40623807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120750946-C-A

40623807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750946-C-G

40623807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750946-C-T

http://identifiers.org/hco/1/GRCh38#40623857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120750898-C-A

40623870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750886-G-A

40623870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750886-G-C

40623886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750870-G-T

40623947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750823-G-T

http://identifiers.org/hco/1/GRCh38#40624037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120750739-C-A

40624358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750511-G-T

http://identifiers.org/hco/1/GRCh38#40624454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120750411-C-A

40624454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750411-C-T

http://identifiers.org/hco/1/GRCh38#40624516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120750365-C-A

40624516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750365-C-T

http://identifiers.org/hco/1/GRCh38#40624600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120750326-C-A

40624600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750326-C-G

40624600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750326-C-T

40624654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750288-G-T

40624736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750236-G-T

40624853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120750150-A-G

40625073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749957-G-A

40625073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749957-G-T

40625138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749896-G-A

40625138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749896-G-T

40625150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749885-A-G

40625366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749692-T-C

40625370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749688-G-T

40625375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749683-G-A

40625423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749634-A-G

40625423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749634-A-T

40625581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749479-G-T

40625958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749216-T-A

40625958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749216-T-C

40625958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749216-T-G

40625963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749202-T-C

40625963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120749202-T-G

http://identifiers.org/hco/1/GRCh38#40626322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120748899-A-C

40626322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748899-A-G

40626322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748899-A-T

http://identifiers.org/hco/1/GRCh38#40626323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120748898-C-A

40626323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748898-C-T

http://identifiers.org/hco/1/GRCh38#40626363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120748858-A-C

40626363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748858-A-G

40626363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748858-A-T

http://identifiers.org/hco/1/GRCh38#40626376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120748845-C-A

40626376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748845-C-T

http://identifiers.org/hco/1/GRCh38#40626377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120748844-C-A

40626377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748844-C-T

40626384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 3 prime UTR variant
orthologous variants: 120748837-G-T

40626593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120748626-T-C

40626787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120748439-G-A

40626787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120748439-G-T

40627032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120748242-C-G

40627032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120748242-C-T

http://identifiers.org/hco/1/GRCh38#40628131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120747471-C-A

40628137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120747465-T-C

40628334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120747304-G-A

http://identifiers.org/hco/1/GRCh38#40628664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120746987-C-A

40628664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746987-C-T

40628672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746979-G-A

40628672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746979-G-T

40628689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746946-G-A

40628689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746946-G-C

40628689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746946-G-T

http://identifiers.org/hco/1/GRCh38#40628747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120746772-A-C

40628874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120746625-G-A

40628874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120746625-G-C

40628961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746538-G-A

40628961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746538-G-C

40628996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746518-G-A

40629121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746401-A-G

40629363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120746192-T-C

40629391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746165-T-C

http://identifiers.org/hco/1/GRCh38#40629427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120746132-C-A

40629427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746132-C-T

40629457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746102-A-T

http://identifiers.org/hco/1/GRCh38#40629500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120746059-C-A

http://identifiers.org/hco/1/GRCh38#40629501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120746058-C-A

40629501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746058-C-T

40629576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120746019-G-A

40630109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120745618-G-A

40630188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120745528-G-A

40633062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120744245-G-A

40633062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120744245-G-C

40633062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120744245-G-T

40633098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120744209-C-T

40633199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120744112-G-C

40633200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120744111-G-A

40633276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120744048-T-A

40633276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120744048-T-C

40633276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120744048-T-G

40634052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120742921-A-G

40634552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120741942-C-G

40634552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120741942-C-T

40634868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120741519-G-A

40635394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740988-A-G

40635674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740698-C-T

40635675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740697-C-G

http://identifiers.org/hco/1/GRCh38#40635742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120740652-C-A

40635792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740625-G-A

40635792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740625-G-T

40635798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740619-G-T

40635803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740614-C-T

40635851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740566-C-G

40635884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740482-G-T

40635886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740480-G-A

40635886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740480-G-T

40635892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740474-A-G

40635892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740474-A-T

http://identifiers.org/hco/1/GRCh38#40636064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120740263-C-A

40636064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120740263-C-T

40636214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120740132-C-T

40636572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739897-G-A

40636601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739873-A-G

40636615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739860-G-A

40636726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739778-T-C

40636726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739778-T-G

40637464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739100-T-A

40637503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120739071-C-T

40639136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120737622-G-A

40639344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120737424-G-A

40639849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120736812-G-C

40640322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120736381-G-T

http://identifiers.org/hco/1/GRCh38#40640350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120736353-A-C

40640390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120736317-T-C

http://identifiers.org/hco/1/GRCh38#40640945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120735782-A-C

40640958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120735769-T-A

40640958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120735769-T-C

40641018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120735709-C-T

40641019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120735708-A-G

40641679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120735311-T-G

40641717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120735272-G-A

http://identifiers.org/hco/1/GRCh38#40641756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120735233-A-C

40641774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120735215-G-A

40641774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: missense variant
orthologous variants: 120735215-G-C

http://identifiers.org/hco/1/GRCh38#40641985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120735004-C-A

40641985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120735004-C-G

40641996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734993-C-G

40641996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734993-C-T

40641997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734992-T-A

40641997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734992-T-C

http://identifiers.org/hco/1/GRCh38#40642006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120734985-C-A

40642013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734978-A-T

http://identifiers.org/hco/1/GRCh38#40642020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120734971-C-A

40642020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734971-C-G

http://identifiers.org/hco/1/GRCh38#40642022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120734969-A-C

40642022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734969-A-G

40642060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734932-T-C

http://identifiers.org/hco/1/GRCh38#40642091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120734896-A-C

40642091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734896-A-T

40642754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734049-G-A

40642754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734049-G-C

40642754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734049-G-T

40642788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120734015-T-A

40644051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120733240-A-G

40644490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120732813-A-G

40644543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120732759-T-C

http://identifiers.org/hco/1/GRCh38#40645156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120731973-C-A

40645348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120731783-T-C

40645383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120731748-G-C

40645657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120731542-T-C

40645756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120731473-C-T

http://identifiers.org/hco/1/GRCh38#40645773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120731456-C-A

40645803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120731427-T-A

40646313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120730770-C-T

http://identifiers.org/hco/1/GRCh38#40646368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120730714-A-C

http://identifiers.org/hco/1/GRCh38#40646872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120730307-A-C

40646872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120730307-A-T

40647237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120730242-C-T

40647426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120730057-G-C

40647918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120729599-C-T

http://identifiers.org/hco/1/GRCh38#40647976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120729539-C-A

40648301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728951-C-T

40648442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728787-C-G

40648450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728779-G-T

40648539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728690-G-C

40648713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728525-G-C

http://identifiers.org/hco/1/GRCh38#40648752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120728486-C-A

40649035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728314-C-T

40649104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728250-G-A

40649124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728228-G-A

http://identifiers.org/hco/1/GRCh38#40649192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120728172-C-A

40649192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120728172-C-T

40649419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727886-C-T

http://identifiers.org/hco/1/GRCh38#40649545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120727759-A-C

40649619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727712-C-T

40649880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727452-A-G

40649900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727434-A-G

40649983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727361-G-A

40650115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727239-T-C

40650286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120727097-G-A

40650918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120726836-T-A

40651060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120726687-A-G

40651132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120726633-G-A

40651164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120726602-T-A

40651191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120726575-C-T

40651464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120726381-T-C

40651937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120725884-T-C

40652200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120725639-C-T

40652305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120725540-G-A

http://identifiers.org/hco/1/GRCh38#40652568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120725289-A-C

40652603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120725257-C-T

http://identifiers.org/hco/1/GRCh38#40652604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120725256-A-C

40652900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120724981-G-A

40653011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120724870-A-G

40653053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120724829-G-A

40653649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120724115-C-G

40653649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120724115-C-T

40653770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120724000-G-T

40653777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723993-A-G

40653839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723927-A-G

http://identifiers.org/hco/1/GRCh38#40654051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120723717-C-A

40654051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723717-C-T

40654060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723698-G-T

40654097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723661-G-T

40654263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723548-G-A

40654263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120723548-G-T

http://identifiers.org/hco/1/GRCh38#40654650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120723249-C-A

40655176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120722832-A-G

40655679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120722085-C-G

40656357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120721308-C-T

40656373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120721291-G-A

40656411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120721263-G-A

40656448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120721217-T-G

http://identifiers.org/hco/1/GRCh38#40657033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120720589-C-A

http://identifiers.org/hco/1/GRCh38#40657571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#120719914-C-A

40658185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120719483-A-T

40658482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120719191-C-T

40658790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120718906-C-T

40658941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120718770-C-T

40659176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120718617-G-A

40659398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120718380-G-T

40659493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120718283-G-A

40659539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120718238-T-C

40659756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120717713-A-G

40661242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120716426-A-G

http://identifiers.org/hco/1/GRCh38#40661432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120716239-C-A

40661510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120716163-T-C

40661527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120716146-C-T

40661580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120716130-A-G

http://identifiers.org/hco/1/GRCh38#40661582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120716128-C-A

40661582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120716128-C-G

40661756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120716030-T-C

40661873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715925-G-T

40662022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715777-A-G

40662106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715691-T-C

40662221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715574-A-T

40662295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715526-T-A

40662347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715480-G-A

40662350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715477-G-A

40662350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715477-G-C

40662607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715235-T-C

40662614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715126-C-T

40662665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120715048-A-T

40662769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120714959-C-T

40662873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120714700-C-T

40663246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120714376-G-A

40663459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120714177-A-T

40663597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120714018-C-G

40663630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120713982-C-T

40663633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120713979-A-T

40663965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120713640-A-G

http://identifiers.org/hco/1/GRCh38#40664263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120713433-C-A

http://identifiers.org/hco/1/GRCh38#40664470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120713242-C-A

http://identifiers.org/hco/1/GRCh38#40664556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120713153-A-C

40665384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120712327-G-A

40665384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120712327-G-C

40665384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120712327-G-T

40665540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120712172-T-A

40665540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120712172-T-C

40665595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120712117-C-T

40665630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 120712081-G-T

40665784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711912-G-A

40665784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711912-G-T

40665817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711887-G-A

40665834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711866-C-T

http://identifiers.org/hco/1/GRCh38#40665838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120711862-A-C

40665838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711862-A-G

40665872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711828-A-G

40665973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120711742-T-C

http://identifiers.org/hco/1/GRCh38#40667123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120709965-C-A

40667123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120709965-C-T

40667169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120709931-T-A

40667262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120709853-A-G

http://identifiers.org/hco/1/GRCh38#40667364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120709762-A-C

40667526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120709545-G-C

40667782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120709328-A-T

40667815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120709285-G-A

40667848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120709239-G-A

40667848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron variant
orthologous variants: 120709239-G-T

40668962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120708381-G-T

http://identifiers.org/hco/1/GRCh38#40668984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120708359-C-A

40669002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120708341-G-A

http://identifiers.org/hco/1/GRCh38#40669096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#120708250-C-A

40669096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21292
most severe consequence: intron_variant, undefined
orthologous variants: 120708250-C-T