http://identifiers.org/hco/15/GRCh38#100400540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66473318-C-A

100400583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66473276-T-A

100400599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66473263-G-C

100400983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472896-A-G

http://identifiers.org/hco/15/GRCh38#100401552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66472739-C-A

100401552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472739-C-T

100401572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472722-G-T

100401657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472634-C-T

100401763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472547-C-G

100401771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472539-A-G

100401794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472525-A-G

100401820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472494-G-T

http://identifiers.org/hco/15/GRCh38#100401848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66472467-C-A

100401848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472467-C-T

100402101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472241-G-A

100402101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472241-G-T

100402107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472235-C-T

100402212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472140-G-A

100402212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472140-G-T

100402236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472101-G-T

100402328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66472014-C-T

http://identifiers.org/hco/15/GRCh38#100402904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66471397-C-A

100402904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66471397-C-G

100408385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66470601-T-C

100408432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66470554-T-C

100408794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66470173-C-T

100408841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66470128-G-T

100408874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66470092-A-G

http://identifiers.org/hco/15/GRCh38#100408937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66470013-A-C

100408937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66470013-A-G

100408975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469985-G-A

100408975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469985-G-T

100409037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469952-G-A

100409357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469151-T-A

100409357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469151-T-G

100409362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469146-G-A

100409362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469146-G-C

100409362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66469146-G-T

100409724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66468817-C-T

100409760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66468783-G-A

100410214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66468078-C-T

100410342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66467961-C-T

100410420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66467890-G-T

100410536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66467788-A-G

http://identifiers.org/hco/15/GRCh38#100412305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66467690-C-A

100412634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66467406-C-T

100413000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66466949-T-C

100413020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66466854-T-A

100413129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66466757-T-G

100413139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66466747-G-A

100413139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66466747-G-T

100413280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66466608-G-T

100426928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66465600-G-C

100427365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66465220-A-G

100427380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66465205-C-T

100427911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66464659-C-T

100427919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66464648-G-A

http://identifiers.org/hco/15/GRCh38#100429558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66463687-C-A

100429562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66463683-C-T

100430398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462810-G-C

100430413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462794-T-G

100430475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462732-C-T

100430500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462709-C-T

100431000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462262-T-C

100431024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462237-C-T

100431035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66462226-T-C

100432275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66460604-C-T

100432478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66460432-T-C

100432489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66460421-A-G

100432542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66460378-T-C

100432542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66460378-T-G

100432663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66460303-G-T

100433465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66454559-C-T

100433894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454220-G-A

100434108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66453973-C-T

100434177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66453908-G-A

100434264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66453868-G-A

100434306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66453829-G-A

100434466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66453673-A-G

http://identifiers.org/hco/15/GRCh38#100434506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66453654-C-A

100434595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66453577-G-A

100435160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66452863-G-A

100436782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66452325-T-C

100437402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451886-C-T

100437421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451868-C-T

100437592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451694-C-T

100437622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451668-A-G

100437769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451569-A-G

http://identifiers.org/hco/15/GRCh38#100437888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66451472-C-A

100437888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66451472-C-T

http://identifiers.org/hco/15/GRCh38#100438450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66450972-A-C

100438450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450972-A-G

100438548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450887-T-A

100438839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450584-A-G

http://identifiers.org/hco/15/GRCh38#100438935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66450490-A-C

100438935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450490-A-G

100439031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450390-G-A

100439049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450372-T-C

100439191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66449881-A-T

100439701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66448876-G-C

100439832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66448744-G-A

100439990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66448591-A-G

100440206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66448378-T-A

http://identifiers.org/hco/15/GRCh38#100455840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66445746-C-A

100455840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445746-C-T

100455844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445742-A-G

100455845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445741-T-C

100455845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445741-T-G

100455930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 66445648-T-C

100456067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445515-G-C

100456067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445515-G-T

100456073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445510-T-C

100456097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445488-A-G

100456176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445410-A-G

100456401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445219-T-C

100456455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445172-G-A

100456542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66445087-A-G

http://identifiers.org/hco/15/GRCh38#100456587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66445040-A-C

100457252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444704-G-A

100457301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444685-A-G

100457320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444666-G-C

100457567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444441-C-T

100457600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444408-T-G

100457706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444304-T-C

100457837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444180-A-G

100460710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440904-C-G

http://identifiers.org/hco/15/GRCh38#100460785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66440811-A-C

100460821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440772-T-A

100460828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440765-G-A

100461148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440346-C-T

100461370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440168-A-T

100461459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440083-T-A

100461559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439976-C-T

100461604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439930-A-G

100469508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439306-G-C

100469508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439306-G-T

100469617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439217-G-A

100469617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439217-G-T

100469626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439209-A-G

http://identifiers.org/hco/15/GRCh38#100469673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66439170-A-C

100469673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66439170-A-G

100470024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66438779-T-G

100470440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66438368-A-G

100470568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66438241-G-T

100470577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66438232-A-T

100471058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437757-C-T

100471216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437600-C-T

100471587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437254-T-C

100471587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437254-T-G

100471624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437217-G-T

http://identifiers.org/hco/15/GRCh38#100471890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66437016-C-A

100471890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437016-C-T

100472099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436618-A-T

100472281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436443-C-T

100472422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436337-C-T

100472638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436160-C-T

100472677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436121-A-G

100472690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436108-G-A

http://identifiers.org/hco/15/GRCh38#100472749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66436055-A-C

100472800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436015-T-G

100472829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435986-A-G

100472829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435986-A-T

100473083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435726-A-G

100473098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435711-T-C

http://identifiers.org/hco/15/GRCh38#100473193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66435543-C-A

100473193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435543-C-T

100473203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435533-G-A

100473203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435533-G-T

100475294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66435352-T-G

100475735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434928-G-T

100475980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66434717-G-A

100475980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66434717-G-T

http://identifiers.org/hco/15/GRCh38#100475991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66434706-C-A

100475991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66434706-C-T

100476060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66434641-A-G

100476289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434425-A-G

100476324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434402-G-A

100476324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434402-G-T

100476374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434352-G-C

100476429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434298-C-T

100476435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434292-G-A

100476733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434169-T-A

100476780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434125-A-G

100476786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434119-T-C

100476876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66434022-C-T

100477102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433892-A-G

100477217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433788-A-T

100479467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 66433159-T-C

100479522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433115-T-C

http://identifiers.org/hco/15/GRCh38#100479941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66431643-C-A

100480082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431504-A-G

100480095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431482-T-A

100485045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428768-T-C

100485368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428441-A-G

100485387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428420-G-A

100485387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428420-G-C

100485958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428150-G-A

100485958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428150-G-T

100486058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428069-C-T

100486082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66428043-C-T

100486260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66427072-T-C

100486393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426942-C-T

100486814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426526-G-C

100486837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426505-C-T

100486891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66426451-T-C

http://identifiers.org/hco/15/GRCh38#100488438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66425697-C-A

100488703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425455-A-G

100488856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66425296-A-T

100489726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424586-A-T

100490065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424266-G-C

100490239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424129-T-C

http://identifiers.org/hco/15/GRCh38#100490253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66424115-A-C

100490253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424115-A-G

100490338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66424029-T-G

100490387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423979-C-T

100490715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423556-G-A

100490756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423516-A-T

100490777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423495-A-G

100490984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423291-T-C

100491015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423259-G-A

100491015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423259-G-C

100491015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66423259-G-T

100491141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422383-C-T

100491200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422324-A-G

100491424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422242-A-G

100491424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422242-A-T

100491477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422189-A-G

100491477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422189-A-T

100491613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422060-G-A

100491613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422060-G-C

100491641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66422032-G-T

100496764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66418452-C-G

100499314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66416926-C-T

http://identifiers.org/hco/15/GRCh38#100499848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66416323-A-C

100499914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66416259-C-T

100500217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415899-T-G

100500221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415895-G-T

100500261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415744-T-C

100500325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415687-A-G

100500332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415680-T-C

100500333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415679-A-G

http://identifiers.org/hco/15/GRCh38#100500360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66415657-C-A

100500378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415639-G-A

100500378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415639-G-T

100500393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415625-G-A

100500403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415615-G-T

100500460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415568-G-A

100500460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415568-G-T

100500468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66415560-T-C

100500508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66415496-C-G

100500508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66415496-C-T

100500520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415484-G-C

100500520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415484-G-T

100500669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415252-G-A

100500689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415233-A-G

100500752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415172-C-G

100500752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66415172-C-T

100500955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66414983-A-G

http://identifiers.org/hco/15/GRCh38#100501640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66414131-A-C

100501948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66413820-T-C

100502482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66413640-A-G

100505082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66412387-G-A

100505372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66412108-T-C

100505438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66412017-G-A

100507469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409945-C-G

100507546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409871-C-T

100507676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409761-C-G

100507676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409761-C-T

100507777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409653-A-G

http://identifiers.org/hco/15/GRCh38#100508557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66409370-C-A

100508557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409370-C-T

http://identifiers.org/hco/15/GRCh38#100508700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66409230-C-A

100508700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409230-C-T

100508701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66409229-A-G

http://identifiers.org/hco/15/GRCh38#100510022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66408573-C-A

100510216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66408385-C-T

100510455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66408000-T-A

100510494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66407962-T-C

100510644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66407810-T-C

100515461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66407581-C-T

100515681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66407382-T-A

100515759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66407303-T-C

100516094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66406969-A-T

100516473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66406612-G-A

100516496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66406590-T-C

100516496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66406590-T-G

http://identifiers.org/hco/15/GRCh38#100516503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66406583-C-A

http://identifiers.org/hco/15/GRCh38#100516852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66406284-C-A

100516885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66406252-A-G

100516899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66406238-G-C

100517823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405411-G-A

100517823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405411-G-C

100517849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405392-G-A

100518035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66405210-G-A

100520305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403774-C-G

100520305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403774-C-T

100520343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403735-G-A

100520355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403723-C-T

100520497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403625-G-A

100521267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403216-A-G

100521367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403120-G-A

100521367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403120-G-C

100521519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66403004-T-C

http://identifiers.org/hco/15/GRCh38#100521567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66402957-A-C

100521623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66402900-G-A

100521724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66402767-T-C

100521935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66402631-G-A

100522022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66402548-T-C

100522040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66402523-C-T

100522080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66402483-A-G

100522635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401976-T-C

100522635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401976-T-G

100522654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401960-G-C

100522806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401826-T-G

http://identifiers.org/hco/15/GRCh38#100522843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66401791-C-A

100522843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401791-C-T

100522962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401681-C-T

100523369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66401198-T-A

100523759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400655-T-C

100524203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400263-A-G

100524229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400237-G-A

100524332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400119-T-C

100524336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66400115-T-C

100525118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399348-T-C

100525176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66399214-C-G

100525311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398879-T-C

100525444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398737-G-A

http://identifiers.org/hco/15/GRCh38#100525461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66398720-C-A

100525475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398706-A-G

100525504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398677-T-C

100525512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398669-G-C

100525531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398653-C-T

http://identifiers.org/hco/15/GRCh38#100525581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66398620-C-A

100525642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398566-T-C

100525642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398566-T-G

http://identifiers.org/hco/15/GRCh38#100525745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66398465-A-C

100525754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398456-C-T

100526107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398098-T-C

100526129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66398075-C-T

http://identifiers.org/hco/15/GRCh38#100526433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66397404-C-A

http://identifiers.org/hco/15/GRCh38#100526626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66397208-A-C

100526791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66397062-C-G

http://identifiers.org/hco/15/GRCh38#100526869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66396986-A-C

100527883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66394438-G-C

100528352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393887-T-C

100528505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393763-C-T

100528686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393591-T-C

100528719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393567-G-A

100528719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393567-G-T

100528727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393559-A-G

100528766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393537-T-C

100528767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66393536-T-C

100528839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66393468-G-A

100528861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66393446-A-G

100528910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66393405-A-G

100529224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66393085-C-T

100529262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66393043-C-T

http://identifiers.org/hco/15/GRCh38#100529296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66393006-C-A

http://identifiers.org/hco/15/GRCh38#100529310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66392984-C-A

100529321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392973-A-G

100529390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392887-C-T

http://identifiers.org/hco/15/GRCh38#100529396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66392881-C-A

100529477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392796-T-A

100529564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392708-T-C

100529565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392707-A-G

http://identifiers.org/hco/15/GRCh38#100529846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66392309-C-A

100529856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392299-T-C

http://identifiers.org/hco/15/GRCh38#100529861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66392294-C-A

100529861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392294-C-T

100529880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392275-G-C

100529899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392256-T-C

100529992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66392163-G-A

100531133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66391186-T-C

100531172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 66391160-A-G

100531482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390838-A-G

100531504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390816-C-T

100531579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390722-A-G

http://identifiers.org/hco/15/GRCh38#100531661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66390633-A-C

http://identifiers.org/hco/15/GRCh38#100531669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66390625-C-A

100531709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390590-T-C

100531715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390584-T-C

100531925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390386-T-C

100531963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66390337-C-T

http://identifiers.org/hco/15/GRCh38#100532025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66390226-A-C

100532936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66389163-A-G

100532938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66389161-T-A

100533955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388572-A-G

100534026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388517-C-G

100534071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388472-C-T

100534163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66388395-G-T

100536709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387626-G-A

100536721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387614-T-C

100536727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387608-C-T

100536943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387411-C-T

100537015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66387350-A-G

100537198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386316-T-A

100537199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386315-G-A

100537255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386259-A-G

100537317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66386197-A-G

100540185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385611-G-A

100540955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66385144-A-G

100542422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384982-A-G

100542434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384970-C-T

100542470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384939-T-C

100542486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384928-A-G

100542543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384872-T-C

100543797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384393-T-C

100543813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384374-T-A

100543813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384374-T-C

100543950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384248-A-G

100543971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384231-G-C

http://identifiers.org/hco/15/GRCh38#100544064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66384142-C-A

100544064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66384142-C-T

100544140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66384081-T-C

100544210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66384029-A-G

100544230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66384009-G-A

100544230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66384009-G-T

http://identifiers.org/hco/15/GRCh38#100544237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66384002-C-A

100544237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66384002-C-G

100544237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66384002-C-T

http://identifiers.org/hco/15/GRCh38#100544240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383999-C-A

100544240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383999-C-G

100544240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383999-C-T

http://identifiers.org/hco/15/GRCh38#100544241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383998-C-A

100544311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383901-G-A

100544329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383885-T-C

100544407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383758-G-T

100544433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383665-G-T

http://identifiers.org/hco/15/GRCh38#100544458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383632-A-C

100544458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383632-A-G

100544458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383632-A-T

100544494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383587-G-T

100544507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383568-G-A

100544507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383568-G-T

100544517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383524-G-A

100544517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383524-G-T

100544538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383499-G-T

http://identifiers.org/hco/15/GRCh38#100544606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383421-C-A

100544606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383421-C-T

100544685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383346-A-G

100544686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383345-G-A

100544686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383345-G-T

100544691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383340-G-T

100544692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 66383339-G-T

http://identifiers.org/hco/15/GRCh38#100544701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383329-C-A

100544728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383298-G-A

100544745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383283-C-G

100544745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383283-C-T

100544763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383270-G-A

100544763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383270-G-T

http://identifiers.org/hco/15/GRCh38#100544782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383257-C-A

100544782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66383257-C-T

http://identifiers.org/hco/15/GRCh38#100544800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383240-C-A

http://identifiers.org/hco/15/GRCh38#100544846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23752
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#66383191-A-C