http://identifiers.org/hco/8/GRCh38#25184696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68170989-C-A

25184696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170989-C-T

25184747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 68170931-G-A

http://identifiers.org/hco/8/GRCh38#25184784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68170884-C-A

25184784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170884-C-G

25184784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170884-C-T

http://identifiers.org/hco/8/GRCh38#25184850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68170831-C-A

25184850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170831-C-T

25184854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170827-G-A

25184854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170827-G-C

25184854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170827-G-T

http://identifiers.org/hco/8/GRCh38#25184855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68170826-C-A

25184855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170826-C-G

25184855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 5 prime UTR variant
orthologous variants: 68170826-C-T

http://identifiers.org/hco/8/GRCh38#25185014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68170683-C-A

25185014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170683-C-G

25185014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170683-C-T

25185025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170672-G-A

25185025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170672-G-C

25185025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170672-G-T

25185059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170656-T-C

25185135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170601-A-G

25185191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170577-C-G

25185603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170262-G-C

25185603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68170262-G-T

25185632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68170236-C-T

25186815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68169258-T-C

25188058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68167713-C-G

25188115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68167656-G-A

25188945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68166462-G-A

25195517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68161706-G-A

25195692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68161524-G-A

25195762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68161459-G-A

25195762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68161459-G-C

25196227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68161076-C-T

25196465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68160842-A-G

25196868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68160428-G-A

25197141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68160274-G-A

25198121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68159458-T-G

25199052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68157517-C-T

25199205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68157344-G-A

25199295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68157259-T-A

25199963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68156927-A-G

25200105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68156848-T-C

25200421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68156558-A-G

http://identifiers.org/hco/8/GRCh38#25201534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68155064-A-C

http://identifiers.org/hco/8/GRCh38#25201602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68154997-A-C

25201624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154974-A-T

25202477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154472-A-T

25202492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154457-C-T

25202554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154392-A-G

25202554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154392-A-T

25202576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154370-G-A

25202612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68154340-T-C

25203107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68153980-C-T

http://identifiers.org/hco/8/GRCh38#25203211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68153905-A-C

25203590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68153528-T-C

25203633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68153479-G-T

25203638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68153474-T-C

25203696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68153429-T-G

25203946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68153007-A-G

http://identifiers.org/hco/8/GRCh38#25203970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68152985-A-C

25204012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68152938-A-T

25204104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68152840-A-G

25204590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68152009-C-T

25204729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68151668-C-T

25204923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68151490-T-G

25204975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68151433-A-T

25205307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68150114-T-G

http://identifiers.org/hco/8/GRCh38#25205698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68149765-C-A

25205811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149651-C-T

25205849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149608-A-G

25206049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149486-G-A

25206059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149475-T-C

25206117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149434-G-C

25206311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149230-C-T

25206409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149123-T-C

25206431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68149101-A-G

25206769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68148800-C-G

25206924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68148652-A-G

25206943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68148633-T-C

25208969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147824-G-T

25209126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147675-G-A

25209131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147670-C-T

25209376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147431-A-G

http://identifiers.org/hco/8/GRCh38#25210868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68147092-C-A

25210868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147092-C-G

25210868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147092-C-T

25210880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147080-A-G

25210880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147080-A-T

25210940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147053-G-C

25210987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68147009-C-T

25213257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144517-G-A

25213310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144460-T-A

25213310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144460-T-C

25213363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144406-G-A

25213363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144406-G-C

25213363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144406-G-T

25213411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144370-C-T

25213574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68144239-A-G

http://identifiers.org/hco/8/GRCh38#25213646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68144170-C-A

25214394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68143698-G-A

25214803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68142854-C-T

25214806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68142851-G-A

25214835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68142823-C-T

25215097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68142320-T-C

25215276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68142151-A-G

25215683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68141877-A-G

25215683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68141877-A-T

25215684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68141876-T-C

25217458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68141061-C-G

25222073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68139230-G-A

25222115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68139190-C-T

25222174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68139130-C-G

25222223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68139089-T-C

25222281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68139048-A-G

25222522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68138824-G-A

http://identifiers.org/hco/8/GRCh38#25226969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68136522-A-C

http://identifiers.org/hco/8/GRCh38#25227003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68136496-C-A

25227101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136391-T-G

25227105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136387-C-T

25227194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136310-C-T

25227275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136230-G-A

25227287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136219-A-T

http://identifiers.org/hco/8/GRCh38#25227299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68136214-A-C

25227391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136006-G-A

25227397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68136000-T-C

25227454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68135940-T-C

25227668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68135741-G-T

25229702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68129522-G-A

25229798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68129448-A-G

25234058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68128777-C-T

25234184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68128615-T-C

25234462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68128023-T-A

25234480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68128004-A-G

25234633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68127864-T-A

25234633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68127864-T-C

25234992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68127522-A-T

http://identifiers.org/hco/8/GRCh38#25235101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68127410-C-A

25235114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68127397-T-C

25235734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68127149-T-C

http://identifiers.org/hco/8/GRCh38#25236140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68126867-A-C

25236305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126709-G-A

25236362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126654-C-T

25236381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126635-T-C

25236396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126620-T-C

25236434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126584-A-T

25236929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126277-T-C

25237424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126118-A-G

25237452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68126098-C-T

25237992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68125511-C-G

25238043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68124760-A-G

25238243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68124587-A-G

25238253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68124577-T-C

25239295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122848-C-G

25239317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122823-A-G

25239325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122815-G-A

25239327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122813-G-A

25239339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122801-G-A

http://identifiers.org/hco/8/GRCh38#25239341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68122799-A-C

25239341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122799-A-G

25239345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122795-G-A

25239349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122791-G-A

25239591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122518-A-G

25239885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122209-C-T

25239965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122119-T-C

25240047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68122061-C-G

25240160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68121965-T-C

25240233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68121902-G-A

25240301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68121849-C-T

http://identifiers.org/hco/8/GRCh38#25242836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68119569-C-A

25242945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68119459-C-G

25242945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68119459-C-T

25243579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118874-T-A

25243579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118874-T-C

http://identifiers.org/hco/8/GRCh38#25243635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68118771-C-A

25243635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118771-C-T

25243636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118770-A-G

25243724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68118679-G-A

25243787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118617-G-A

http://identifiers.org/hco/8/GRCh38#25243791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68118613-A-C

25243816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118588-A-T

25243844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118560-A-G

http://identifiers.org/hco/8/GRCh38#25243854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68118550-C-A

25243859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118543-T-C

25243866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118536-G-A

25243910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118488-A-G

http://identifiers.org/hco/8/GRCh38#25243960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68118440-A-C

http://identifiers.org/hco/8/GRCh38#25243982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68118418-A-C

25244135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118288-A-G

25244141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118282-C-T

25244273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68118155-G-C

25244602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68117850-A-G

25244651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68117826-C-T

25244999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68117507-G-A

25247737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68116257-C-T

25247819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68116169-C-T

http://identifiers.org/hco/8/GRCh38#25248038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68115963-A-C

25248288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68115737-G-A

25248603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68115412-A-G

http://identifiers.org/hco/8/GRCh38#25248730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68115287-C-A

25249951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68114762-T-C

http://identifiers.org/hco/8/GRCh38#25250124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68114595-A-C

25250193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68114533-G-A

25250583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68114160-A-G

25250614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68114130-T-C

25251038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113719-C-T

25251085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113673-G-A

25251314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113482-T-C

25251347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113449-T-C

25251464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113342-C-G

25251464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113342-C-T

25251495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68113313-C-T

25252515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68112655-G-A

25252515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68112655-G-C

25252637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68112490-T-C

25260061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110863-A-G

http://identifiers.org/hco/8/GRCh38#25260175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68110755-C-A

25260175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110755-C-T

25260563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110364-G-A

25260901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110135-T-A

25260901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110135-T-C

25261149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110104-T-C

25261180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68110073-A-G

25261407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68109862-G-A

25261664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68109601-T-G

25261665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68109600-G-A

25261764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68109538-C-T

25261792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68109511-G-A

25263928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106960-C-T

25263946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106942-A-G

25264074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106821-A-G

25265400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106332-T-C

25265452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106282-G-T

25265472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106262-C-T

25265533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106202-T-A

25265533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68106202-T-C

25265864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105938-A-G

25265889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105913-C-T

25266049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105792-A-G

25266056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105785-C-T

http://identifiers.org/hco/8/GRCh38#25266518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68105296-C-A

25266557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105259-C-T

25266645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105177-C-T

25266648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68105174-A-G

25266888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104914-C-T

25267080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104737-A-T

25267209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104617-T-G

25267235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104591-G-A

25267235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104591-G-C

25267304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104540-A-G

25267411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104451-T-C

25267471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104397-G-T

25267493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104375-A-G

25267546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104325-A-G

25267934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68104041-C-T

25268728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103643-T-C

http://identifiers.org/hco/8/GRCh38#25268729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68103642-C-A

25268729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103642-C-G

http://identifiers.org/hco/8/GRCh38#25268737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68103638-A-C

25268737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103638-A-G

http://identifiers.org/hco/8/GRCh38#25268749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68103626-C-A

25268749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103626-C-T

25268833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103542-T-C

25268860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68103504-A-G

25268860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68103504-A-T

25268861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: stop gained
orthologous variants: 68103503-T-A

25268861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: synonymous variant
orthologous variants: 68103503-T-C

25268862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68103502-A-G

25268889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103475-T-C

25268925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103443-T-C

http://identifiers.org/hco/8/GRCh38#25268928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68103440-C-A

25268954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103415-A-G

25268966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103403-G-A

25268966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103403-G-T

http://identifiers.org/hco/8/GRCh38#25269029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68103348-C-A

25269080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103297-G-A

25269092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103285-A-G

25269096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68103281-A-G

25269445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102963-C-T

25269509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102907-T-C

25269509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102907-T-G

25269643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102776-T-C

25269986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102471-A-G

25270034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102415-C-T

25270100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102319-A-G

25270190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68102224-C-T

25270521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68101709-T-G

25270538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68101688-T-A

http://identifiers.org/hco/8/GRCh38#25270800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68101260-C-A

25270801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 68101259-C-T

25270853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, missense_variant
orthologous variants: 68101205-T-C

25271223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68101097-C-G

http://identifiers.org/hco/8/GRCh38#25271353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68100820-C-A

25271360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68100813-A-G

25271472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68100523-T-C

25271584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68100415-G-A

25271713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68100309-T-C

25273881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68098562-G-C

25273917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68098532-A-T

25274046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68098449-A-G

25274286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68098220-A-G

25274389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68098107-C-T

25274401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68098095-C-T

25274660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097843-A-G

25274660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097843-A-T

25274671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097833-G-C

25275132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097636-G-A

25275162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097606-C-G

http://identifiers.org/hco/8/GRCh38#25275171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68097597-C-A

http://identifiers.org/hco/8/GRCh38#25275179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68097589-A-C

25275201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097567-G-C

http://identifiers.org/hco/8/GRCh38#25275239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68097527-C-A

25275239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097527-C-G

25275239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097527-C-T

25275297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097466-A-G

25275356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097430-G-T

http://identifiers.org/hco/8/GRCh38#25275357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68097429-C-A

25275357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097429-C-T

25275371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097415-T-G

25275425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68097362-A-G

25276041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68097122-A-G

25277799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68096054-A-G

25277805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68096048-A-G

25277829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68096021-G-A

http://identifiers.org/hco/8/GRCh38#25277953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68095969-C-A

25278126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095840-G-A

25278132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095834-G-T

http://identifiers.org/hco/8/GRCh38#25278174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68095807-C-A

25278174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095807-C-T

25278450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095581-C-T

25278531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095483-A-G

25278533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095481-C-T

25278548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095467-C-T

25278615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68095400-C-T

25278639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68095376-G-T

25278851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68095172-T-C

25279419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094357-A-G

25280108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094266-C-G

25280219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094152-G-T

25280245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094127-G-A

25280262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094110-C-T

25280360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094069-A-G

25280422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68094010-A-T

25280625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68093831-A-G

25282107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68092026-G-A

25282273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68091938-C-T

http://identifiers.org/hco/8/GRCh38#25282417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68091806-A-C

25282891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68091339-A-T

25282893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68091337-G-T

25282974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68091258-G-T

http://identifiers.org/hco/8/GRCh38#25283014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68091222-C-A

25283023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68091213-C-G

25283023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68091213-C-T

25283305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68090893-G-A

25283309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68090889-T-C

25283398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68090800-T-C

25283838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68090379-T-C

25283838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68090379-T-G

25284044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68090201-A-G

http://identifiers.org/hco/8/GRCh38#25285417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68089711-A-C

25285435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089696-A-G

25285713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089441-C-T

25285727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089429-T-C

25286090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089222-G-A

25286151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089194-C-T

25286227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089141-G-A

25286272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089098-G-A

25286272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089098-G-T

25286283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089087-G-A

25286290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68089068-C-G

25286557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68088866-G-A

25287449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68088193-A-G

25287449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68088193-A-T

25287522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68088171-T-G

25287557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68088140-G-C

http://identifiers.org/hco/8/GRCh38#25287748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68087941-A-C

25287823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68087862-A-G

http://identifiers.org/hco/8/GRCh38#25288662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68086361-A-C

25288806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68086216-C-G

25288806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68086216-C-T

25288915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68086128-A-G

25288915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68086128-A-T

25288948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68086101-G-A

25288976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68086072-A-G

25289060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68085989-G-A

http://identifiers.org/hco/8/GRCh38#25289121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68085933-C-A

25289276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68085780-C-G

25289622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68085570-C-T

25290087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68085152-A-G

25290102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68085127-T-C

25290114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68085116-C-T

25290603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68084655-T-C

25290683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68084579-T-G

25292002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083605-T-G

25292011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083596-T-C

25292099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68083509-T-A

25292099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68083509-T-G

25292150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68083458-G-A

25292150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68083458-G-T

25292209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083404-G-A

25292209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083404-G-T

25292214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083399-A-G

http://identifiers.org/hco/8/GRCh38#25292222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68083391-C-A

25292222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083391-C-T

http://identifiers.org/hco/8/GRCh38#25292228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68083385-C-A

25292246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083369-T-A

25292246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68083369-T-C

25292332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68082378-A-T

25292362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68082347-C-T

25294084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68081473-G-A

http://identifiers.org/hco/8/GRCh38#25296446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68080414-C-A

25296446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68080414-C-T

25296607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68080253-G-A

25296607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68080253-G-C

25296751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68080100-G-A

http://identifiers.org/hco/8/GRCh38#25296756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68080095-C-A

25296756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68080095-C-T

25296840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68080026-G-A

25296939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68079923-A-G

25298845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68078698-G-A

25298884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68078662-T-A

25298927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68078631-G-A

25298927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68078631-G-T

http://identifiers.org/hco/8/GRCh38#25299040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68078518-A-C

http://identifiers.org/hco/8/GRCh38#25299112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68078446-C-A

http://identifiers.org/hco/8/GRCh38#25299167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68078395-C-A

25299167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078395-C-T

http://identifiers.org/hco/8/GRCh38#25299228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68078332-C-A

25299228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078332-C-G

25299228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078332-C-T

25299236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078324-T-A

25299236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078324-T-C

25299248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078312-T-C

25299373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68078011-T-C

25299459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68077939-G-T

25299484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077914-A-G

http://identifiers.org/hco/8/GRCh38#25299500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68077898-C-A

25299500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077898-C-T

25299557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077836-T-C

http://identifiers.org/hco/8/GRCh38#25299669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68077771-A-C

25299870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077589-T-A

25299896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077567-A-G

25300106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077477-A-G

25300196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077406-G-A

http://identifiers.org/hco/8/GRCh38#25300314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68077289-A-C

25300314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077289-A-G

25300463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077184-T-C

25300553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68077100-G-T

25300622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, missense_variant
orthologous variants: 68077029-A-G

25301375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68074786-A-G

25301536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68074625-C-G

25301948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68074222-T-C

http://identifiers.org/hco/8/GRCh38#25302196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68073969-C-A

25302196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073969-C-G

25302196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073969-C-T

25302222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073943-T-A

25302379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68073836-G-T

25302400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: synonymous variant
orthologous variants: 68073815-C-T

http://identifiers.org/hco/8/GRCh38#25302505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68073713-A-C

25302529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073685-T-G

http://identifiers.org/hco/8/GRCh38#25302573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68073619-C-A

25302573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073619-C-G

25302573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073619-C-T

http://identifiers.org/hco/8/GRCh38#25302580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68073611-A-C

25302580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073611-A-G

25302592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073599-G-T

25302593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073598-A-G

25302593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073598-A-T

25302693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073508-C-T

25302879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073296-G-A

25302939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073244-T-C

25303054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68073139-A-G

25303236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68072936-C-T

25303454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68072755-G-T

25304097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68069874-C-G

25304097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68069874-C-T

http://identifiers.org/hco/8/GRCh38#25304181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68069814-A-C

25304181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68069814-A-G

25304181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68069814-A-T

25304272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68069720-A-G

http://identifiers.org/hco/8/GRCh38#25304302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68069690-A-C

http://identifiers.org/hco/8/GRCh38#25304357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68069636-C-A

25304362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069631-G-A

25304362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069631-G-T

25304403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069583-G-C

25304403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069583-G-T

25304450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069532-G-A

25304450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069532-G-T

25304518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069469-G-A

25304518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069469-G-T

25304539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069447-T-C

25304558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069437-G-T

http://identifiers.org/hco/8/GRCh38#25304587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68069400-C-A

25304587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069400-C-T

25304616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069371-G-T

25304625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069362-G-A

25304625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069362-G-T

25304790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069205-G-A

25304841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069155-G-T

25304889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069124-G-A

25304889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069124-G-T

25304901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069114-G-A

25304901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069114-G-T

25304951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069071-G-T

25304952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069070-A-G

25304983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069041-T-C

25304987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68069037-G-A

http://identifiers.org/hco/8/GRCh38#25305118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68068911-C-A

25305118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 68068911-C-T

25306316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: -C-T

25306348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: -T-C

25307814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067786-A-T

25307888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067749-T-C

25307986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067664-C-T

25308012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067640-T-C

25308105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067555-C-T

25308246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067417-T-C

25308250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067413-A-G

http://identifiers.org/hco/8/GRCh38#25308278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68067389-A-C

25308303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067364-T-C

25308341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067351-G-C

25308431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68067284-C-G

25308566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68067154-G-T

http://identifiers.org/hco/8/GRCh38#25308710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68066022-C-A

25308727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68066005-C-T

25308732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68066000-G-A

25308829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 68065904-C-T

25308844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 68065889-C-G

http://identifiers.org/hco/8/GRCh38#25308973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68065758-A-C

25308973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065758-A-G

http://identifiers.org/hco/8/GRCh38#25309034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68065705-C-A

25309034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065705-C-G

http://identifiers.org/hco/8/GRCh38#25309036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68065703-C-A

25309036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065703-C-T

25309042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065697-G-A

25309042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065697-G-T

http://identifiers.org/hco/8/GRCh38#25309045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68065694-A-C

25309045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065694-A-G

25309055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065684-T-A

25309055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065684-T-C

25309055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 68065684-T-G

25310081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68062486-G-A

25310559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68062004-T-C

25310559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68062004-T-G

25311570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68061383-A-G

25312043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68061177-T-A

25312044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68061176-G-T

25312046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68061174-G-T

25316703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060659-C-T

25316838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060266-A-T

25316896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060225-A-G

25316896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060225-A-T

25316917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060206-G-A

25316917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060206-G-C

25316917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060206-G-T

25316975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060149-G-A

25316996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 68060128-T-A

25317078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68060046-A-G

25317093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68060031-A-G

25317142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68059982-T-C

25317187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68059939-A-G

25317210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68059894-T-A

http://identifiers.org/hco/8/GRCh38#25317220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68059848-C-A

25317230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68059840-G-A

25317230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68059840-G-T

http://identifiers.org/hco/8/GRCh38#25317242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68059825-C-A

25317286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68059773-T-A

25317384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68059684-G-A

25317384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68059684-G-T

25317460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68059643-A-G

25317489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68059614-A-T

25317516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68059586-C-T

25319552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058890-T-C

25319614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense_variant, undefined
orthologous variants: 68058828-T-A

25319684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 68058758-T-A

25319684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 68058758-T-C

25319692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058757-T-C

http://identifiers.org/hco/8/GRCh38#25319706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68058744-A-C

25319706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058744-A-G

25319707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058743-T-C

25319721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68058729-G-A

http://identifiers.org/hco/8/GRCh38#25319789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68058644-C-A

25319789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058644-C-T

25319792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058641-A-G

25319797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058636-G-A

25319842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058537-A-G

25320093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058271-G-A

25320093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058271-G-C

25320111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058254-A-G

25320297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, undefined
orthologous variants: 68058090-A-G

25320369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68058022-A-T

25320636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057662-G-A

25320662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057635-C-T

25320778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057543-A-G

25320833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057461-G-T

25320880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057376-G-A

25320880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057376-G-C

25320880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057376-G-T

25320882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057374-G-A

25320882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057374-G-T

25321017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68057123-T-A

25321017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68057123-T-C

http://identifiers.org/hco/8/GRCh38#25321085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68057055-C-A

25321134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68057011-A-G

25321155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056998-G-T

25321167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056986-G-A

25321167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056986-G-C

25321167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056986-G-T

25323462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056629-A-G

25323487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056602-G-A

25323496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056593-G-A

25323509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056580-G-C

25323561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056528-A-G

25323574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056513-G-C

25323576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056511-G-T

25323699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056389-A-G

25323737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056350-A-G

25323737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056350-A-T

25323741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056345-G-C

25323741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056345-G-T

http://identifiers.org/hco/8/GRCh38#25323753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68056333-A-C

http://identifiers.org/hco/8/GRCh38#25323759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68056327-C-A

25323759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056327-C-T

25323760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056326-A-G

25323786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056299-T-C

25323789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056296-T-C

25323796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056289-C-T

25323904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68056181-G-A

25323913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: missense variant
orthologous variants: 68056172-A-G

25323955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056130-G-A

25323955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056130-G-T

http://identifiers.org/hco/8/GRCh38#25323962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68056123-C-A

25323971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056103-G-A

25323971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056103-G-T

25324007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056064-G-A

25324060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056012-G-T

25324076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68056001-A-G

25324139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055944-G-A

25324241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055866-A-G

25324251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055856-C-T

25324297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055809-G-T

25324317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055789-A-G

25324356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055746-C-T

25324426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055683-C-T

http://identifiers.org/hco/8/GRCh38#25324432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68055678-C-A

25324581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055521-T-C

25324588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055514-T-C

25324602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055500-G-C

25325132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055380-G-A

25325161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055351-T-C

25325211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055302-A-G

25325233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055287-G-A

25325233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055287-G-T

25325281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055241-G-A

25325287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055233-G-A

25325287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055233-G-T

25325290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron variant
orthologous variants: 68055230-T-C

25325555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 68054952-T-C

25325555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 68054952-T-G

25325557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054950-G-A

25325582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054927-T-G

25325586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054923-G-T

25325621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054888-G-T

25325634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054875-T-A

25325634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054875-T-C

25325662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054847-T-C

25325662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68054847-T-G

25326122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68053949-A-G

25326514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68053583-G-A

25326634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68053456-T-C

25326767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68053379-A-T

http://identifiers.org/hco/8/GRCh38#25331882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68052731-C-A

25331950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68052679-G-A

25331985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68052645-G-A

25332178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051872-A-T

http://identifiers.org/hco/8/GRCh38#25332512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68051559-C-A

25332512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051559-C-T

http://identifiers.org/hco/8/GRCh38#25332536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68051535-C-A

25332536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051535-C-T

25332546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051518-G-A

25332558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051506-T-G

25332618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 68051449-C-T

25332666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 68051401-T-C

25332777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051310-T-C

25332777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051310-T-G

http://identifiers.org/hco/8/GRCh38#25332843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68051245-A-C

25332917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051172-T-A

25332985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68051106-A-G

25333175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68050914-G-A

25333509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68050260-G-A

25333850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049921-C-T

25333880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049891-C-T

25333934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049853-A-G

25333987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049800-C-T

25334015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049773-A-G

25334054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049731-G-A

25334054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049731-G-T

25334068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049717-T-C

http://identifiers.org/hco/8/GRCh38#25334084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68049701-C-A

25334089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 68049696-T-G

25334162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 68049623-A-G

25334237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049547-G-T

25334249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049546-T-C

25334257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049538-G-A

25334257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049538-G-T

http://identifiers.org/hco/8/GRCh38#25334276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68049519-C-A

25334276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049519-C-T

25334277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049518-G-A

25334277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049518-G-T

http://identifiers.org/hco/8/GRCh38#25334280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68049515-C-A

25334516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68049284-G-T

25334991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68048754-A-T

25335152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68048598-G-C

25335188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68048564-C-T

25335189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68048563-C-T

25335706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68047624-A-G

25335768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68047558-T-G

25335823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68047508-T-G

25335870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68047468-C-T

25336089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046732-T-G

25336276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 68046549-G-A

25336286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68046539-C-T

25336378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046447-T-C

25336385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046443-T-C

25336389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046439-G-A

25336402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046432-G-A

25336402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046432-G-C

25336442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046397-G-A

http://identifiers.org/hco/8/GRCh38#25336486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68046346-C-A

25336486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68046346-C-T

25340331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68045644-A-G

25340335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68045640-G-A

25340436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68045541-C-T

25340675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68045354-G-A

25340902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68044795-G-A

25340947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68044750-A-G

http://identifiers.org/hco/8/GRCh38#25340994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68044703-C-A

25340994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044703-C-T

25341042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044653-T-G

25341060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044643-G-A

25341060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044643-G-T

http://identifiers.org/hco/8/GRCh38#25341062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68044641-C-A

25341062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044641-C-T

25341096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044613-A-T

25341115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044594-T-C

25341165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044463-A-T

25341266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044358-A-G

http://identifiers.org/hco/8/GRCh38#25341278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68044346-A-C

25341278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044346-A-G

25341564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044100-A-G

25341626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044047-G-T

25341642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044031-A-G

25341650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68044023-A-T

25341703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043970-T-G

http://identifiers.org/hco/8/GRCh38#25341708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68043966-A-C

25341708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043966-A-G

25341869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043813-C-T

25341912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043776-G-A

25341912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043776-G-C

25341912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043776-G-T

25341918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043766-A-G

http://identifiers.org/hco/8/GRCh38#25341919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68043765-C-A

25341928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043756-T-A

25341928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043756-T-C

http://identifiers.org/hco/8/GRCh38#25341943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68043737-C-A

25341943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043737-C-T

25341957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043723-A-G

25342278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043469-A-G

25342281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043466-T-G

25342283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043464-G-A

25342283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043464-G-T

25342356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043328-T-C

25342429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68043255-A-G

http://identifiers.org/hco/8/GRCh38#25342444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68043240-C-A

25342444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 68043240-C-T

25342512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043168-G-A

25342522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043158-A-G

25342531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043149-G-A

25342531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043149-G-T

http://identifiers.org/hco/8/GRCh38#25342549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68043129-C-A

25342549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68043129-C-T

http://identifiers.org/hco/8/GRCh38#25342570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68043112-C-A

25345308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 68040680-T-A

http://identifiers.org/hco/8/GRCh38#25345369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68040643-A-C

25345369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68040643-A-G

25345369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68040643-A-T

25345378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68040632-A-G

25345378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68040632-A-T

25345408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 68040615-A-G

25345408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 68040615-A-T

http://identifiers.org/hco/8/GRCh38#25345470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#68040571-C-A

25345470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 68040571-C-G

25346941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68039422-A-G

25346980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68039379-A-G

25347026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68039334-G-A

25347042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68039306-C-T

25347244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68039109-G-A

25347292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68039064-C-G

25347463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68038899-T-C

http://identifiers.org/hco/8/GRCh38#25351747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68037869-A-C

25351770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 68037846-C-T

http://identifiers.org/hco/8/GRCh38#25351791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68037825-A-C

25352333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68037657-C-G

25352539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68037468-A-G

25352559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68037448-A-G

25355801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68036416-A-G

25355802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68036415-A-G

25355836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68036382-T-G

25355881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68036339-A-G

25355891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68036325-C-T

25358563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68034127-T-C

25358720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68033756-T-C

25358794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68033672-C-T

25358851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68033616-A-G

25358865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68033602-C-T

25358972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 68033506-G-A

25363002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68031519-G-C

http://identifiers.org/hco/8/GRCh38#25363026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68031498-C-A

http://identifiers.org/hco/8/GRCh38#25363177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68031344-C-A

25363187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68031334-A-G

http://identifiers.org/hco/8/GRCh38#25363210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68031314-A-C

25363253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68031271-G-C

25363283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68031248-T-C

25363287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68031244-T-C

25363415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68031141-T-C

25363999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68030333-A-G

25364164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68030138-T-C

25364268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68030060-C-G

25364272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68030056-T-A

http://identifiers.org/hco/8/GRCh38#25364314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68030017-A-C

25364314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68030017-A-G

25364354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029984-G-A

25364498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029870-A-G

25364500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029868-A-G

25364500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029868-A-T

25364523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029845-G-T

25364524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029844-A-T

25364565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029805-G-A

25364565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029805-G-T

25364607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029763-T-C

25364608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68029762-G-T

25364679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68029693-T-C

25364681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68029691-G-A

25364681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68029691-G-C

25364681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68029691-G-T

25364760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68029623-T-C

25366736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027900-G-A

25366736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027900-G-T

25366745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027880-A-G

25366779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027858-A-T

25366780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027857-A-G

http://identifiers.org/hco/8/GRCh38#25366783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68027854-A-C

25366783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027854-A-G

25366790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027847-A-G

25366912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68027725-C-T

25366933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68027704-A-G

25366960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68027677-A-G

25367084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027376-G-A

http://identifiers.org/hco/8/GRCh38#25367118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68027341-C-A

25367118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68027341-C-T

25367439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68026770-C-T

25367549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68026645-A-G

25367866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68025509-T-G

25367873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68025497-C-T

25367897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68025477-G-A

25368058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68025321-G-T

25368100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68025276-A-T

25368110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68025266-T-A

25368140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68024377-G-T

25368420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68024042-T-C

25368428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68024031-A-G

25368430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68024029-A-G

25368430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68024029-A-T

25368431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68024028-T-G

25368497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023949-C-T

25368515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023930-A-G

25368548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023897-A-G

http://identifiers.org/hco/8/GRCh38#25368550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68023895-C-A

25368552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023893-T-C

25368573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 68023872-C-T

25368684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68023761-C-G

25368684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 68023761-C-T

25368736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023709-G-A

http://identifiers.org/hco/8/GRCh38#25368737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68023708-C-A

25368737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023708-C-T

25368740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023705-A-T

25368753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023694-A-T

http://identifiers.org/hco/8/GRCh38#25368771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68023678-C-A

25368843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023610-G-A

25368843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023610-G-T

25368914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023539-G-T

25368941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68023508-G-A

25369449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022447-G-A

25369480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022418-G-A

25369480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022418-G-C

25369497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022399-G-A

http://identifiers.org/hco/8/GRCh38#25369520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68022366-C-A

25369520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022366-C-T

25369522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022364-A-G

25369598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68022290-G-A

25369613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68022275-G-A

25369613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 68022275-G-T

25369659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022230-G-A

25369659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022230-G-T

25369674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022215-T-A

25369674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022215-T-C

25369726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022181-A-G

25369771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022143-T-A

25369880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022042-G-C

25369901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68022019-G-A

25369980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021942-C-T

25370156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021790-T-C

25370165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021781-T-C

http://identifiers.org/hco/8/GRCh38#25370168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68021778-C-A

25370168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021778-C-T

25370213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021735-A-G

25370242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021706-T-C

25370281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021684-C-T

25371032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021247-T-G

25371191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68021108-A-G

25371698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68020559-T-C

http://identifiers.org/hco/8/GRCh38#25371709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68020548-C-A

25371718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68020535-T-A

25371759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68020498-T-C

25371990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68020048-C-G

25371994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68020044-A-G

25372085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68019984-G-A

http://identifiers.org/hco/8/GRCh38#25372668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68019491-A-C

25372668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68019491-A-G

25372668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68019491-A-T

http://identifiers.org/hco/8/GRCh38#25372704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68019455-A-C

25372704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68019455-A-G

25372704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68019455-A-T

http://identifiers.org/hco/8/GRCh38#25372765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68019394-C-A

25372765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68019394-C-T

25372821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68019349-G-A

25373318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018830-G-T

25373536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018576-G-A

25373536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018576-G-T

25373732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018375-A-G

25373755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018352-G-A

25373755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018352-G-T

25373864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018245-T-C

25373998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68018127-T-C

25374637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68017743-C-G

25374637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68017743-C-T

25374758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 68017615-G-A

25374791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 68017582-T-C

25374831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017543-A-G

http://identifiers.org/hco/8/GRCh38#25374877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017500-A-C

http://identifiers.org/hco/8/GRCh38#25374904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017473-C-A

25374904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017473-C-G

25375016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017375-T-G

http://identifiers.org/hco/8/GRCh38#25375086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017281-A-C

25375086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017281-A-T

http://identifiers.org/hco/8/GRCh38#25375104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017263-C-A

http://identifiers.org/hco/8/GRCh38#25375135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017241-A-C

25375135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017241-A-G

25375135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017241-A-T

http://identifiers.org/hco/8/GRCh38#25375170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017203-A-C

25375170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017203-A-T

25375175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017198-G-A

25375175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017198-G-C

25375175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017198-G-T

25375192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017181-T-A

25375192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017181-T-C

25375192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017181-T-G

25375302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017107-A-G

25375347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017063-G-A

http://identifiers.org/hco/8/GRCh38#25375484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68017016-C-A

25375484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017016-C-G

25375484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017016-C-T

25375523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017015-A-G

25375524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017014-G-A

25375524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68017014-G-T

http://identifiers.org/hco/8/GRCh38#25375620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016958-C-A

25375621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016957-T-C

25375633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016945-C-G

25375633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016945-C-T

http://identifiers.org/hco/8/GRCh38#25375755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016839-C-A

http://identifiers.org/hco/8/GRCh38#25375792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016802-C-A

25375940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016718-A-T

http://identifiers.org/hco/8/GRCh38#25375958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016690-C-A

25375958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016690-C-T

25375987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016662-A-T

http://identifiers.org/hco/8/GRCh38#25375990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016659-C-A

25375990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016659-C-T

25376002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016647-G-A

25376002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016647-G-T

25376110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016592-A-G

25376270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016539-T-G

25376291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016518-T-C

http://identifiers.org/hco/8/GRCh38#25376369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016435-C-A

25376440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016380-G-A

25376440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016380-G-T

25376463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016361-T-A

25376463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68016361-T-C

http://identifiers.org/hco/8/GRCh38#25376509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016339-C-A

http://identifiers.org/hco/8/GRCh38#25376550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68016291-C-A

http://identifiers.org/hco/8/GRCh38#25376623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68015834-A-C

25376686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68015773-G-A

25376686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68015773-G-T

http://identifiers.org/hco/8/GRCh38#25376687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68015772-A-C

25376692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68015767-G-T

25376695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68015764-T-C

http://identifiers.org/hco/8/GRCh38#25376803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68015657-C-A

25376803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 68015657-C-T

http://identifiers.org/hco/8/GRCh38#25376891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68015582-A-C

25376891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015582-A-G

25376928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015547-G-T

25376938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015537-G-A

25376938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015537-G-C

25376938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015537-G-T

25376956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015521-A-G

http://identifiers.org/hco/8/GRCh38#25377006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68015473-C-A

25377244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68015210-T-C

25377300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 68015144-T-G

25377453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68014991-G-A

http://identifiers.org/hco/8/GRCh38#25380240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68013863-C-A

25380244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013859-T-C

25380368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 68013719-G-T

25380461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013636-T-G

25380502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013593-A-G

25380502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013593-A-T

25380509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013586-A-G

25380530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013570-G-A

25380531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013569-A-G

25380531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68013569-A-T

25381272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68012891-A-G

25382553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68012174-T-C

25382593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68012136-A-G

25382647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68012071-C-T

25382902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68011809-G-T

http://identifiers.org/hco/8/GRCh38#25383136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68011591-A-C

25383143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68011584-C-G

25383143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68011584-C-T

25383222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68011511-T-C

25383907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010963-G-C

25384074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010810-A-G

25388979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010750-G-A

25388979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010750-G-T

http://identifiers.org/hco/8/GRCh38#25389019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68010710-C-A

25389019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010710-C-T

25389039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010692-G-T

25389221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68010510-C-G

http://identifiers.org/hco/8/GRCh38#25389265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68010466-C-A

25389265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010466-C-T

25389323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010409-C-T

25389537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68010240-T-G

http://identifiers.org/hco/8/GRCh38#25389816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68009541-C-A

25389816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68009541-C-T

http://identifiers.org/hco/8/GRCh38#25389840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68009520-C-A

25389840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68009520-C-G

25390128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68009284-A-G

25390261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68009162-T-A

25390274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68009149-G-A

25390274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68009149-G-C

25390274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 68009149-G-T

http://identifiers.org/hco/8/GRCh38#25390390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68009079-C-A

25390390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68009079-C-T

25390429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68009042-G-A

25390586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008929-G-A

25390660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008860-T-C

25391694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008706-C-G

25391694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008706-C-T

25391744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008658-C-T

http://identifiers.org/hco/8/GRCh38#25391746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68008656-C-A

25391746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008656-C-G

25391746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008656-C-T

http://identifiers.org/hco/8/GRCh38#25391747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68008655-A-C

25391747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008655-A-G

25391747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008655-A-T

25391768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008636-A-G

25391777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008627-G-A

25391777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008627-G-C

25391777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008627-G-T

25391791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008624-G-A

25391791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008624-G-T

http://identifiers.org/hco/8/GRCh38#25391809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68008605-C-A

25391882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68008553-T-C

25392722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007812-T-C

http://identifiers.org/hco/8/GRCh38#25392727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68007807-A-C

25392823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68007738-A-G

25392898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007663-T-C

25392950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007558-G-A

25392950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007558-G-T

25393176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007325-T-C

25393277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007238-C-T

25393456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 68007031-C-T

http://identifiers.org/hco/8/GRCh38#25395460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68004959-C-A

25395621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68004798-C-T

25395648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 68004771-C-T

25395772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68004664-G-A

25395778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 68004658-C-T

http://identifiers.org/hco/8/GRCh38#25395810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68004632-C-A

http://identifiers.org/hco/8/GRCh38#25395861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68004610-A-C

25395861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68004610-A-G

25395965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68004534-A-T

25395977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68004520-T-C

25395993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68004504-G-A

25396020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68004483-A-G

25396406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68004087-G-T

25396525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003891-A-G

25396822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003695-C-T

25396948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003578-C-T

http://identifiers.org/hco/8/GRCh38#25399833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68003459-C-A

25399833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003459-C-G

25399833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003459-C-T

http://identifiers.org/hco/8/GRCh38#25399974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68003324-A-C

25400024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003253-G-A

25400024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003253-G-T

http://identifiers.org/hco/8/GRCh38#25400031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68003246-C-A

25400031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003246-C-T

http://identifiers.org/hco/8/GRCh38#25400033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68003244-C-A

25400033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68003244-C-T

http://identifiers.org/hco/8/GRCh38#25400056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68003220-C-A

http://identifiers.org/hco/8/GRCh38#25400782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68002323-A-C

25400782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002323-A-G

25400833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002272-G-A

25400833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002272-G-C

25400833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002272-G-T

http://identifiers.org/hco/8/GRCh38#25400846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68002262-C-A

25400846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002262-C-T

http://identifiers.org/hco/8/GRCh38#25400849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68002259-C-A

25400849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002259-C-T

25400877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002230-A-G

25400884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002223-C-G

25400884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002223-C-T

25400895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002212-G-A

25400992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 68002115-C-T

25401072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002035-C-T

25401081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68002026-A-G

25401118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001997-T-G

25401342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001806-A-G

25401353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001798-G-A

http://identifiers.org/hco/8/GRCh38#25401389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68001764-C-A

25401389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001764-C-T

25401390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001763-G-A

25401390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001763-G-C

25401395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68001758-A-G

25403515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000816-T-C

25403588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68000743-C-G

25403588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 68000743-C-T

http://identifiers.org/hco/8/GRCh38#25403749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68000585-A-C

25403749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000585-A-G

25403753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000581-A-G

http://identifiers.org/hco/8/GRCh38#25403792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#68000520-C-A

25403792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000520-C-G

25403792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000520-C-T

25403827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000478-A-G

25403864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 68000448-G-T

25407469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996832-G-A

25407525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996777-G-C

25408170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996410-G-A

25408170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996410-G-T

http://identifiers.org/hco/8/GRCh38#25408174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67996406-A-C

25408174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996406-A-G

http://identifiers.org/hco/8/GRCh38#25408233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67996336-C-A

25408233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996336-C-T

25408255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996310-T-C

25408255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996310-T-G

http://identifiers.org/hco/8/GRCh38#25408272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67996293-C-A

25408338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67996231-G-A

http://identifiers.org/hco/8/GRCh38#25408385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67996182-C-A

25408596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995967-C-T

25408637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995910-G-A

http://identifiers.org/hco/8/GRCh38#25408650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67995897-C-A

25408650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995897-C-T

25408653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995894-T-G

25408733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995633-T-C

25408755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995575-A-G

25408960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995364-T-C

25409109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995222-C-T

25409320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995079-G-T

25409343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995056-G-A

25409343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 67995056-G-T

25409464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994941-T-G

25409489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994916-G-C

25409489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994916-G-T

25409585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994864-A-G

25410031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994717-A-G

25410037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994711-A-G

25410037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994711-A-T

25410072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994677-G-A

25410072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 67994677-G-T

25410121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67994633-T-A

25410130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67994624-G-A

25410130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67994624-G-C

25410243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994512-A-G

25410272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994483-A-G

25410289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994465-G-C

25410289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994465-G-T

25410301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994453-G-C

http://identifiers.org/hco/8/GRCh38#25410314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67994438-A-C

25410314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994438-A-G

25410342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994410-A-G

25410423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994336-C-T

25410424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994335-G-A

http://identifiers.org/hco/8/GRCh38#25410502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67994301-C-A

25410502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994301-C-T

25410534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994288-T-C

25410919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994187-C-G

25410919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994187-C-T

http://identifiers.org/hco/8/GRCh38#25411017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67994132-A-C

25411017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994132-A-G

25411017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994132-A-T

25411048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994106-G-A

25411048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994106-G-C

25411124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994031-A-G

25411130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994025-G-A

25411130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67994025-G-T

25411164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67993998-G-A

25411164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67993998-G-T

25411186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67993976-T-C

http://identifiers.org/hco/8/GRCh38#25411226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67993937-C-A

25411299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993864-G-A

25411299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993864-G-T

25411386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993775-T-C

25411414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993747-G-C

25411414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993747-G-T

25411493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993724-C-T

25411499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993718-A-G

25411511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993708-A-G

25411569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993661-T-A

25411569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993661-T-C

25411578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993652-A-G

25411646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993578-A-G

http://identifiers.org/hco/8/GRCh38#25411649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67993575-C-A

25411649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993575-C-T

http://identifiers.org/hco/8/GRCh38#25411650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67993574-C-A

25411650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993574-C-T

25411679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993547-T-A

25411679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993547-T-C

25411764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993468-A-T

25411809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 67993424-T-C

http://identifiers.org/hco/8/GRCh38#25411858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67993377-A-C

25411886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67993349-T-C

25412019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67993287-G-T

25412117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67993217-C-T

25412128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67993206-T-A

25412141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67993193-G-A

25412174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67993158-T-C

25412192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67993140-G-A

25412287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67993052-T-G

25412299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67993040-T-C

25412370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992963-A-T

25412414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992915-G-T

25412479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992848-T-C

25412635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992644-G-A

25412635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992644-G-T

http://identifiers.org/hco/8/GRCh38#25412636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67992643-C-A

http://identifiers.org/hco/8/GRCh38#25412699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67992589-C-A

http://identifiers.org/hco/8/GRCh38#25412788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67992526-C-A

25412789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992525-T-C

25412833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992500-A-G

25412833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992500-A-T

25412855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992470-T-C

http://identifiers.org/hco/8/GRCh38#25412862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67992463-C-A

25412917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992409-C-T

25412982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992354-T-C

25412991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992345-A-G

25412999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992337-G-A

25413054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992312-A-G

25413102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992284-T-G

25413107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992279-G-T

25413372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67992061-C-T

25413566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67991884-G-A

http://identifiers.org/hco/8/GRCh38#25413624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67991840-C-A

25413637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67991823-G-T

25413803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67991477-G-T

25413841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67991437-G-T

25414169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67991040-A-G

25414169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67991040-A-T

25414297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990941-G-T

http://identifiers.org/hco/8/GRCh38#25414344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67990894-C-A

25414353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990885-G-T

25414485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990757-A-T

25414535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990704-G-T

25414647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990611-T-C

http://identifiers.org/hco/8/GRCh38#25414733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67990532-C-A

http://identifiers.org/hco/8/GRCh38#25414735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67990530-C-A

25414816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990448-A-G

25414816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990448-A-T

25415206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990140-T-C

25415225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990123-T-A

25415225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67990123-T-C

25415472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67989803-C-T

25415501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67989769-G-C

25415501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67989769-G-T

25415538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67989739-G-A

25415803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67989492-C-G

25415838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67989458-T-C

25415946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67989349-T-G

25415953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67989342-C-T

25417626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988673-G-A

25417705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988599-A-G

25417776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988533-T-G

25417788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67988521-T-C

http://identifiers.org/hco/8/GRCh38#25418077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#67988306-C-A

25418077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23476
most severe consequence: non coding transcript exon variant
orthologous variants: 67988306-C-T