86106224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71885746-A-G

http://identifiers.org/hco/2/GRCh38#86106226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#71885744-A-C

http://identifiers.org/hco/2/GRCh38#86106239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71885731-A-C

86106262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71885705-T-A

86106262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71885705-T-C

86106262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71885705-T-G

http://identifiers.org/hco/2/GRCh38#86106269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71885698-C-A

86106269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71885698-C-G

86106269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71885698-C-T

http://identifiers.org/hco/2/GRCh38#86106275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#71885692-C-A

86106275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 71885692-C-T

86106278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71885689-G-A

86106278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71885689-G-C

86106278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 71885689-G-T

86106560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71885433-C-T

86106667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71885326-T-C

86106892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71885102-C-G

86106902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71885092-A-G

86106929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71885060-C-T

86108473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71884701-T-C

86108473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71884701-T-G

86110779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882607-T-C

86110859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882523-A-G

86110859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882523-A-T

http://identifiers.org/hco/2/GRCh38#86110863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71882519-C-A

86110863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882519-C-T

http://identifiers.org/hco/2/GRCh38#86110882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71882496-C-A

86110882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882496-C-T

86110933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882440-T-C

86110961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882268-T-G

86110962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882267-T-C

86111021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71882195-T-G

86111134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71882104-G-A

86111134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71882104-G-T

86115870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880942-C-T

86115923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880888-T-C

86116503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880503-A-G

86116504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880502-G-T

86116522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71880484-T-G

86116551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71880455-G-C

86116575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71880431-A-G

86116575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71880431-A-T

86116588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71880418-C-G

86116618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880388-T-A

http://identifiers.org/hco/2/GRCh38#86116633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71880366-C-A

86116633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880366-C-G

86116689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880301-G-C

86116962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880034-T-A

86116962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71880034-T-G

86117012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71879990-T-A

86117012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71879990-T-C

86117169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71879828-G-A

http://identifiers.org/hco/2/GRCh38#86118801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71878381-C-A

86118888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71878333-T-C

86118893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71878328-A-G

86118893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71878328-A-T

http://identifiers.org/hco/2/GRCh38#86118902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71878320-A-C

86118902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71878320-A-G

86118942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71878280-G-A

86119301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877943-G-A

86119301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877943-G-T

86119324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877918-G-A

86119324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877918-G-T

86119580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71877632-T-A

86119623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877567-T-C

86120093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877109-C-G

86120093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877109-C-T

86120103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71877099-T-C

86121419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71875493-A-G

86121429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71875483-A-T

http://identifiers.org/hco/2/GRCh38#86121468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71875448-C-A

86121468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71875448-C-G

86121468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71875448-C-T

86121699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71875233-G-C

86121699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71875233-G-T

86123561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874260-G-T

http://identifiers.org/hco/2/GRCh38#86123667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71874173-A-C

86123667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874173-A-G

86123667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874173-A-T

http://identifiers.org/hco/2/GRCh38#86123733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: coding_sequence_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#71874109-A-C

86123811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874048-T-C

86123834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874023-G-A

86123834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874023-G-T

86123840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874017-G-A

86123840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71874017-G-T

86124948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71873021-T-C

86125148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872142-A-G

http://identifiers.org/hco/2/GRCh38#86125149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71872141-C-A

86125149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872141-C-G

86125149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872141-C-T

86125154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872136-A-G

86125158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872132-T-A

86125158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872132-T-G

86125176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872116-G-A

86125176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872116-G-T

http://identifiers.org/hco/2/GRCh38#86125187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71872107-C-A

86125198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872095-T-C

86125200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872093-G-T

86125206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872080-T-C

86125218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872068-G-T

http://identifiers.org/hco/2/GRCh38#86125229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71872057-A-C

86125229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71872057-A-G

http://identifiers.org/hco/2/GRCh38#86125317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71871965-C-A

86125317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871965-C-G

86125347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871935-G-A

86125473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71871845-G-A

86125480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71871838-A-G

86125486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71871832-A-G

http://identifiers.org/hco/2/GRCh38#86125509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71871809-C-A

86125688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871449-G-C

86125688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871449-G-T

86125694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871448-T-G

86125705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871437-G-A

86125705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871437-G-T

86125868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71871281-G-T

86125910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871230-A-G

86125910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71871230-A-T

86127042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71870611-A-G

86127042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71870611-A-T

86127082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71870573-T-G

http://identifiers.org/hco/2/GRCh38#86127206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71870463-C-A

86127217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71870452-T-A

86127288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71870381-T-G

86127308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71870361-G-A

86127308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71870361-G-T

http://identifiers.org/hco/2/GRCh38#86127509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71869872-A-C

86127509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869872-A-G

86127533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869846-C-G

86127533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869846-C-T

86127632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869747-A-G

86127635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869744-T-C

86127656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869728-G-T

86127743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869658-A-G

86127785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869622-G-C

86127785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869622-G-T

86127804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869603-T-A

86127804-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869603-T-G

86127907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71869541-T-C

86129904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71867070-C-G

86130615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71866709-T-C

86130647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 71866669-G-A

86130651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71866662-A-G

86130654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71866659-C-T

http://identifiers.org/hco/2/GRCh38#86130828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71866497-C-A

86130828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71866497-C-T

http://identifiers.org/hco/2/GRCh38#86130858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71866481-A-C

86130911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71866450-C-G

86131024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71866406-T-A

86131072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71866357-T-C

http://identifiers.org/hco/2/GRCh38#86131144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71866268-C-A

86131162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71866250-G-A

http://identifiers.org/hco/2/GRCh38#86131205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71866224-C-A

86131205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71866224-C-T

86132235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71865728-A-G

86132244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71865714-T-C

86132258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71865700-A-G

86132258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71865700-A-T

86132281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71865679-G-A

86132409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71865554-A-G

86132415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71865548-A-G

86133079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71862658-T-G

http://identifiers.org/hco/2/GRCh38#86133095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71862638-A-C

86133095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71862638-A-T

86133173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71862563-C-T

86133209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71862527-G-A

86133269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71862467-A-G

86133406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71862321-C-T

http://identifiers.org/hco/2/GRCh38#86133547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71862215-C-A

86133547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71862215-C-G

http://identifiers.org/hco/2/GRCh38#86133570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71862192-C-A

86133570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71862192-C-T

86134165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861721-T-C

http://identifiers.org/hco/2/GRCh38#86134210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71861692-A-C

http://identifiers.org/hco/2/GRCh38#86134211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71861691-C-A

86134246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861654-G-T

http://identifiers.org/hco/2/GRCh38#86134270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71861627-C-A

86134270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861627-C-T

86134277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861620-C-G

86134277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861620-C-T

http://identifiers.org/hco/2/GRCh38#86134476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71861435-C-A

86134476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861435-C-T

http://identifiers.org/hco/2/GRCh38#86134482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71861429-C-A

86134491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861420-G-A

86134491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71861420-G-T

86134639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71860732-A-G

86134894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71860519-A-G

http://identifiers.org/hco/2/GRCh38#86134994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71860419-A-C

86135003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860410-C-T

86135057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860359-G-A

86135057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860359-G-T

http://identifiers.org/hco/2/GRCh38#86135079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71860330-C-A

86135079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860330-C-T

86135113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860299-T-A

86135113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860299-T-C

86135171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860244-G-A

86135171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860244-G-T

86135191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71860233-T-A

86135297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71860130-G-T

86135302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71860125-G-A

86135302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71860125-G-T

86135333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71860094-T-A

86135732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71859817-C-T

86135949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71859596-G-T

86135959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71859586-G-C

86135959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71859586-G-T

86136396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71859332-T-A

86136567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859165-G-T

http://identifiers.org/hco/2/GRCh38#86136627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71859089-C-A

http://identifiers.org/hco/2/GRCh38#86136669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71859063-A-C

86136669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859063-A-G

86136674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859058-T-C

86136702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859030-T-G

86136709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859023-G-A

86136709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859023-G-C

86136709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71859023-G-T

86136937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron variant
orthologous variants: 71858692-A-G

86137025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense variant
orthologous variants: 71858603-A-G

86137393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron variant
orthologous variants: 71858286-G-A

86137393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: intron variant
orthologous variants: 71858286-G-T

86137490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: synonymous variant
orthologous variants: 71858192-T-C

86137539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: missense variant
orthologous variants: 71858146-G-A

86137558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: stop lost
orthologous variants: 71858136-G-C

86137558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: stop lost
orthologous variants: 71858136-G-T

86138275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71857265-A-G

86138552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71857079-T-C

86138660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71856979-G-A

86138741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71856920-A-T

86139144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71856634-G-T

http://identifiers.org/hco/2/GRCh38#86140242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71855255-A-C

http://identifiers.org/hco/2/GRCh38#86140243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#71855254-A-C

86140251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71855235-T-A

86140251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71855235-T-G

86141353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71854383-C-T

86141428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71854308-T-C

86141471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24717
most severe consequence: 3 prime UTR variant
orthologous variants: 71854265-T-C