146149447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97986283-T-G

146149558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97986174-G-C

146149758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985980-G-T

146149925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985701-T-C

146150189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985262-T-A

146150189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985262-T-C

146150303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985143-A-G

146150313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985134-G-T

146150317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985130-T-G

146150381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97985030-C-G

http://identifiers.org/hco/1/GRCh38#146152849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97984279-C-A

146152851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97984277-T-A

146153290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97983923-T-A

146153292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97983921-G-A

146153687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97983109-G-T

146153718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97983081-A-G

146153756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97983049-T-G

146153951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97982903-C-G

http://identifiers.org/hco/1/GRCh38#146154052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97982856-C-A

146154052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97982856-C-T

146154333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97982584-C-T

146154413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97982503-A-G

146154505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97982472-C-T

146154572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97982440-A-G

146154616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97982397-C-G

146155420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97981295-G-A

146155612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97981094-T-C

http://identifiers.org/hco/1/GRCh38#146155844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97980870-A-C

146156163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97980540-T-G

146156342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 97980380-T-G

146156439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 97980277-G-A

146156467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, missense_variant
orthologous variants: 97980249-G-A

146156521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97980195-C-T

146156696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97980020-A-G

146156731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97979985-G-A

http://identifiers.org/hco/1/GRCh38#146156843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97979873-C-A

146156843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979873-C-G

146156843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979873-C-T

146156846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979870-G-A

146156886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979823-T-C

146156941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979774-G-A

146156977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979738-G-C

146156989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97979726-G-C

http://identifiers.org/hco/1/GRCh38#146157153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97979566-C-A

146164631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97978870-A-T

http://identifiers.org/hco/1/GRCh38#146164638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97978863-A-C

146164641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97978860-G-A

146164685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97978497-T-C

146164689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97978493-A-G

146164738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97978446-T-C

http://identifiers.org/hco/1/GRCh38#146164759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97978425-C-A

146164759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978425-C-G

146164759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978425-C-T

146164787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978397-C-G

146164828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978356-C-T

146164852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978332-G-A

146164852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978332-G-C

146164852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978332-G-T

146164900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978284-G-A

146164900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978284-G-T

146164951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 97978233-C-T

146165662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97977544-T-A

146166091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97977047-G-A

146166327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97976882-C-T

146166669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97976556-G-C

146167884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97975003-A-G

146169942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97972205-C-T

http://identifiers.org/hco/1/GRCh38#146170330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97971830-C-A

146173971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971513-T-C

http://identifiers.org/hco/1/GRCh38#146173981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97971502-C-A

146173987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971496-C-T

146174151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971386-T-C

146174159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971378-T-C

146174201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971350-T-C

146174210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971341-G-A

http://identifiers.org/hco/1/GRCh38#146174331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97971224-A-C

146174397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971165-T-C

http://identifiers.org/hco/1/GRCh38#146174558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97971017-C-A

146174558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97971017-C-G

146174674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97970907-T-C

146174770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97970811-G-A

146174770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97970811-G-C

146174770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97970811-G-T

146174776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97970807-G-C

146174776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97970807-G-T

146175749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97969708-G-C

146176077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97969385-G-T

146176178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97969284-T-C

146176297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97969196-T-A

146176491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97969019-A-G

http://identifiers.org/hco/1/GRCh38#146176675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97968777-C-A

146176677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97968775-C-T

http://identifiers.org/hco/1/GRCh38#146176693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97968759-C-A

http://identifiers.org/hco/1/GRCh38#146177579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97965652-C-A

146177579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97965652-C-T

146177640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97965591-G-C

146178055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97965260-T-C

http://identifiers.org/hco/1/GRCh38#146178063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97965252-A-C

146178315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97965013-G-C

146178373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97964972-A-G

146178713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97964452-T-C

146178760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97964405-G-C

146179413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963796-T-C

146179504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963705-T-C

146180239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963385-T-C

146180257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963374-C-T

146180448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963212-T-G

146180487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963178-C-T

146180573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97963104-T-A

146180744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97962906-T-A

146180744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97962906-T-C

http://identifiers.org/hco/1/GRCh38#146181418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97962374-C-A

146182102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97961792-C-G

146182160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97961653-T-G

146182319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97961516-G-A

146182388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97961442-T-C

146183138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97961015-C-G

146183138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97961015-C-T

http://identifiers.org/hco/1/GRCh38#146183206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97960967-C-A

146183247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97960895-G-T

146183263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97960880-C-T

146183267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97960877-C-T

146183495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97960391-T-C

146183629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97960260-A-G

146184875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97959061-G-T

146184990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97958953-A-G

146185021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97958924-T-G

146185530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97958492-G-A

146185530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97958492-G-C

146185530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97958492-G-T

146185948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97958080-T-A

http://identifiers.org/hco/1/GRCh38#146186033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97958007-C-A

http://identifiers.org/hco/1/GRCh38#146186098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97957956-A-C

146187638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97956419-T-C

146187810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97956290-T-C

146187835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97956279-T-G

146188304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97955771-A-G

146188382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97955693-T-C

146188395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97955680-T-C

146188412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97955665-A-G

http://identifiers.org/hco/1/GRCh38#146188417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97955660-A-C

146189335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, missense_variant, start_lost
orthologous variants: 97955088-C-G

146189436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97954987-A-G

http://identifiers.org/hco/1/GRCh38#146196137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97950921-C-A

http://identifiers.org/hco/1/GRCh38#146196940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97950116-A-C

146197003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97950071-C-T

146197208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97949888-G-T

146197609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97949361-A-G

146197898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97949168-C-G

146197898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97949168-C-T

146197923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97949135-A-G

146198218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97948823-T-C

146198400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97948437-A-G

http://identifiers.org/hco/1/GRCh38#146198710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97948144-C-A

146198710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97948144-C-T

146198740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97948114-A-T

146198763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97948091-G-A

146198763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97948091-G-T

146199285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97947850-G-A

146203496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97944840-G-T

http://identifiers.org/hco/1/GRCh38#146203728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97944615-C-A

http://identifiers.org/hco/1/GRCh38#146203744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97944599-C-A

146204405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97943540-A-G

146205031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942948-T-C

http://identifiers.org/hco/1/GRCh38#146205032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97942947-C-A

http://identifiers.org/hco/1/GRCh38#146205275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97942697-C-A

146205329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942665-G-T

146205350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942650-T-C

http://identifiers.org/hco/1/GRCh38#146206210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97942472-C-A

http://identifiers.org/hco/1/GRCh38#146206255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97942422-A-C

146206273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942405-C-G

146206329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942349-A-G

146206500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942196-C-G

146206560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97942133-G-A

146209232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97941012-C-T

146209331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940918-T-C

146209655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940592-C-T

146209659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940588-C-T

146209694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940556-A-G

146209694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940556-A-T

146209773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, undefined
orthologous variants: 97940478-G-A

146209818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940414-A-G

146209886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940350-T-C

146210020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97940217-A-G

146210623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939534-A-G

146210688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939444-A-G

146210810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939217-A-G

146210810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939217-A-T

146210811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939216-T-A

146210811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939216-T-C

146210821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939206-A-G

146210821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939206-A-T

146210825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939202-T-A

146210825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97939202-T-C

146210935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97939115-G-A

146210935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97939115-G-T

146210976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97939074-G-A

146211067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97938982-T-C

146211840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97937963-G-T

http://identifiers.org/hco/1/GRCh38#146219272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97931489-C-A

146219961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97929552-A-G

146219975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97929538-T-C

146221691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97927768-C-G

146221694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97927765-A-G

146221772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97927681-C-G

146221790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97927664-C-T

146221884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97927585-T-C

146222133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97927341-T-C

146223211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97925802-T-G

http://identifiers.org/hco/1/GRCh38#146223900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97925166-A-C

146224176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97925011-T-A

146224176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97925011-T-C

146224444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97924853-T-A

146225011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97924378-G-C

146225017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97924372-T-C

146225356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97924025-T-C

146226044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97923416-A-G

146226080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, undefined
orthologous variants: 97923396-G-A

146226080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, undefined
orthologous variants: 97923396-G-C

http://identifiers.org/hco/1/GRCh38#146226239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97923294-C-A

146226262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97923264-A-G

146227196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97922359-C-T

http://identifiers.org/hco/1/GRCh38#146228118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#97921314-C-A

146228118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921314-C-T

146228153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921279-G-A

146228153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921279-G-C

146228156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921276-G-A

146228211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, undefined
orthologous variants: 97921222-C-T

146228360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron_variant, undefined
orthologous variants: 97921196-T-C

146228407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 97921186-G-C

146228460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97921146-G-A

146228630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921117-G-A

146228630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921117-G-C

146228630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: intron variant
orthologous variants: 97921117-G-T

146229018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97920833-G-A

146229018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97920833-G-C

146229018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31862
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97920833-G-T