http://identifiers.org/hco/1/GRCh38#33145524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804999-C-A

33145544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804979-A-G

http://identifiers.org/hco/1/GRCh38#33145548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804973-C-A

33145548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804973-C-T

http://identifiers.org/hco/1/GRCh38#33145651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804879-C-A

33145651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804879-C-T

http://identifiers.org/hco/1/GRCh38#33145652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804878-C-A

33145681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804849-G-T

http://identifiers.org/hco/1/GRCh38#33145694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804836-C-A

http://identifiers.org/hco/1/GRCh38#33145709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804817-C-A

33145712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804814-T-C

33145716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804810-C-G

33145716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804810-C-T

33145802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804666-T-C

http://identifiers.org/hco/1/GRCh38#33145817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804651-A-C

http://identifiers.org/hco/1/GRCh38#33145822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804646-C-A

33145822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804646-C-T

http://identifiers.org/hco/1/GRCh38#33145843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804623-C-A

http://identifiers.org/hco/1/GRCh38#33145846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804620-C-A

33145875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804578-T-C

http://identifiers.org/hco/1/GRCh38#33145959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804493-C-A

33145983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804462-G-A

33145983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804462-G-T

33146079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804395-G-A

33146136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804337-T-C

http://identifiers.org/hco/1/GRCh38#33146202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804268-C-A

http://identifiers.org/hco/1/GRCh38#33146231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804240-C-A

http://identifiers.org/hco/1/GRCh38#33146281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804195-A-C

33146281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804195-A-G

http://identifiers.org/hco/1/GRCh38#33146289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804187-C-A

33146289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804187-C-G

33146289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804187-C-T

33146291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804185-G-A

33146291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804185-G-T

33146297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804179-A-G

33146297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804179-A-T

33146309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804167-T-G

http://identifiers.org/hco/1/GRCh38#33146322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804153-A-C

http://identifiers.org/hco/1/GRCh38#33146346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804127-C-A

33146346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804127-C-T

33146428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804043-A-G

33146437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804034-G-T

http://identifiers.org/hco/1/GRCh38#33146472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128804011-C-A

33146472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128804011-C-T

33146557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803936-A-G

http://identifiers.org/hco/1/GRCh38#33146689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128803829-A-C

http://identifiers.org/hco/1/GRCh38#33146694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128803824-C-A

33146694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803824-C-T

33146782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803738-T-C

33146782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803738-T-G

33146803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803717-C-T

33146808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803712-T-C

33146808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803712-T-G

33146823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803698-G-A

33146823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803698-G-T

http://identifiers.org/hco/1/GRCh38#33146830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128803691-C-A

http://identifiers.org/hco/1/GRCh38#33146831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128803690-C-A

33146831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803690-C-T

33146837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803684-T-C

33146837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803684-T-G

33146840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803681-G-C

33146863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803655-G-A

33146867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803651-G-A

33146883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803637-T-A

33146883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803637-T-C

33146883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803637-T-G

33146893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803627-G-A

33146893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803627-G-T

33147014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803546-A-G

33147136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 128803418-T-C

33147388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant
orthologous variants: 128803166-C-T

33147439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant
orthologous variants: 128803115-A-G

33147475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant
orthologous variants: 128803079-C-G

33147673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant
orthologous variants: 128802881-G-A

33147673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, stop_gained
orthologous variants: 128802881-G-T

http://identifiers.org/hco/1/GRCh38#33147945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128802641-A-C

33148127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128802500-G-A

33148128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128802499-T-A

33148180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128802481-G-A

33148363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128802301-A-G

33148422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128802253-T-C

33148530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128802169-T-C

33149041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128801491-G-A

http://identifiers.org/hco/1/GRCh38#33149075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128801459-C-A

33149952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128801221-C-G

33150111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128801066-A-G

33150134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128801043-C-T

33150143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128801035-G-C

33150319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128800858-C-T

http://identifiers.org/hco/1/GRCh38#33150487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128800687-C-A

33150614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128800579-G-A

33150761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128800417-G-C

33150845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128800333-T-G

33151381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128799570-G-A

33151393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128799558-G-A

http://identifiers.org/hco/1/GRCh38#33151536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128799329-C-A

33151765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128799124-T-C

33151858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128799042-C-T

http://identifiers.org/hco/1/GRCh38#33152072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128798896-A-C

33152918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128798384-T-G

33152922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128798380-C-T

33152937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, undefined
orthologous variants: 128798366-G-A

33153492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128797853-G-A

33153493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128797852-C-G

33153907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128797429-C-G

33158255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 128796377-G-A

33158489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128796199-G-A

33158489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128796199-G-C

33158489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128796199-G-T

33158503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128796184-A-G

33158805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128795811-C-T

33159564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794705-G-T

33159627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794649-G-A

33159627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794649-G-T

33159636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794640-G-A

33159636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794640-G-C

33159636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794640-G-T

33159652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794630-G-T

33159672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794609-G-A

33159672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794609-G-T

33159676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794605-G-C

33159676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron variant
orthologous variants: 128794605-G-T

33159709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128794572-C-T

33159724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128794557-T-G

http://identifiers.org/hco/1/GRCh38#33159781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128794500-C-A

33159781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128794500-C-T

33159829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128794452-G-A

33159829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128794452-G-T

33159832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128794449-C-T

33159985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794286-G-C

33159998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794274-C-T

33160054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794229-G-A

33160054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794229-G-T

33160061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794222-C-G

33160061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794222-C-T

33160069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794214-G-A

33160069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794214-G-C

33160069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794214-G-T

33160071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794212-G-A

33160071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794212-G-T

33160073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128794210-A-G

33161149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128793660-G-A

33161343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128793516-G-C

33161515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128793364-G-T

http://identifiers.org/hco/1/GRCh38#33162567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792899-A-C

33162615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792856-G-A

33162615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792856-G-T

33162702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792775-G-A

33162702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792775-G-T

33162716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792761-A-G

33162725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792752-T-G

33162736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792741-A-G

33162736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792741-A-T

33162738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792739-T-C

33162738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128792739-T-G

http://identifiers.org/hco/1/GRCh38#33163591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792397-C-A

33163591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792397-C-T

http://identifiers.org/hco/1/GRCh38#33163615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792380-C-A

33163637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792359-A-G

33163638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792358-G-A

33163638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792358-G-T

http://identifiers.org/hco/1/GRCh38#33163664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792334-C-A

http://identifiers.org/hco/1/GRCh38#33163710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792293-C-A

http://identifiers.org/hco/1/GRCh38#33163717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792288-C-A

33163717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792288-C-T

http://identifiers.org/hco/1/GRCh38#33163718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792287-C-A

33163747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792256-G-A

33163747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792256-G-T

33163767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792233-G-A

33163768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792232-G-T

33163770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792230-G-A

33163776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792224-G-A

33163776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792224-G-T

33163870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792131-T-A

33163870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792131-T-C

33163887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792115-G-A

33163887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792115-G-C

33163887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792115-G-T

33163893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792109-G-A

33163893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792109-G-C

33163893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128792109-G-T

http://identifiers.org/hco/1/GRCh38#33164001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128792006-C-A

http://identifiers.org/hco/1/GRCh38#33164040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128791979-C-A

33164040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791979-C-G

33164040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791979-C-T

33164069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791956-A-G

33164069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791956-A-T

33164137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791895-C-T

33164232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791804-C-T

http://identifiers.org/hco/1/GRCh38#33164234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128791802-C-A

33164260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791775-G-T

33164444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791618-G-C

33164466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791594-G-A

33164481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791575-A-G

33164635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791462-G-A

33164635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791462-G-C

33164635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791462-G-T

33164707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791374-G-T

33164828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791220-G-T

33164931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791164-T-A

33164931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791164-T-C

http://identifiers.org/hco/1/GRCh38#33165131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128791002-C-A

33165131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791002-C-T

33165132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128791001-A-T

http://identifiers.org/hco/1/GRCh38#33165138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790994-C-A

33165138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790994-C-T

33165190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790946-A-G

http://identifiers.org/hco/1/GRCh38#33165261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790887-C-A

http://identifiers.org/hco/1/GRCh38#33165310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790847-C-A

33165310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790847-C-G

http://identifiers.org/hco/1/GRCh38#33165351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790805-C-A

33165375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790781-A-T

http://identifiers.org/hco/1/GRCh38#33165377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790779-C-A

33165377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790779-C-T

http://identifiers.org/hco/1/GRCh38#33165428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790752-C-A

33165428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790752-C-G

33165428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790752-C-T

http://identifiers.org/hco/1/GRCh38#33165438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790742-C-A

33165438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790742-C-T

http://identifiers.org/hco/1/GRCh38#33165443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790737-C-A

33165443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790737-C-T

33165459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790718-G-A

33165459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790718-G-T

http://identifiers.org/hco/1/GRCh38#33165626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790560-C-A

33165626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790560-C-G

33165626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790560-C-T

http://identifiers.org/hco/1/GRCh38#33165642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790544-C-A

33165642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790544-C-G

33165642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790544-C-T

33165651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790535-T-C

33165652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790534-T-C

33165652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790534-T-G

http://identifiers.org/hco/1/GRCh38#33165656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790530-C-A

33165656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790530-C-T

http://identifiers.org/hco/1/GRCh38#33165669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128790518-C-A

33165669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128790518-C-T

33166871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128789162-T-C

33166990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128789030-C-G

33167046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128788971-C-T

http://identifiers.org/hco/1/GRCh38#33167286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128788765-A-C

33167328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128788738-T-C

33167511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128788596-G-A

33168412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128787506-G-T

33168480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128787436-G-A

33168520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128787411-G-A

33168719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128787238-G-A

33168719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128787238-G-C

33169180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128786874-C-G

33169180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128786874-C-T

http://identifiers.org/hco/1/GRCh38#33169379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128786697-C-A

33169878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128786240-C-T

33169983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128786121-T-G

33170020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128786083-T-C

33170476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128785815-C-T

33170595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128785679-C-G

33170675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128785595-G-T

33170709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128785562-T-C

33170729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128785542-A-T

33171557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128784874-T-C

33172333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128784012-G-A

33172477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128783905-T-G

33172667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128783749-G-A

33172796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128783656-G-C

33173045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128783532-C-G

33173088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128783516-C-T

33173522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128783181-T-C

http://identifiers.org/hco/1/GRCh38#33174643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128782980-A-C

33174801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782842-C-T

33175475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782635-G-A

33175500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782615-C-G

33175587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782548-G-A

33175725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782439-G-A

33175752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782412-T-C

33175780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782384-C-G

33176213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128782049-G-A

33176490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128781766-G-A

33176490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128781766-G-T

33176495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128781761-G-A

33176498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128781758-G-T

33176538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128781719-T-C

33176538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128781719-T-G

http://identifiers.org/hco/1/GRCh38#33176596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128781671-C-A

33176739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128781476-A-G

33176952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128781315-G-A

33176967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128781297-C-G

33176967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128781297-C-T

33177137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128781199-G-A

33177372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128780970-C-G

http://identifiers.org/hco/1/GRCh38#33177406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128780949-C-A

33177437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128780924-G-A

33179764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128779804-G-A

33179764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128779804-G-T

http://identifiers.org/hco/1/GRCh38#33180349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128778956-C-A

33180349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128778956-C-G

33180923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128778440-T-A

33180923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128778440-T-C

33180923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128778440-T-G

33181215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 128778178-T-C

http://identifiers.org/hco/1/GRCh38#33181388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128778005-C-A

33181388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128778005-C-G

33181388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 128778005-C-T

http://identifiers.org/hco/1/GRCh38#33181941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#128777488-C-A

33181941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25574
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 128777488-C-T