69244372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110160159-C-T

69244679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 110160476-T-C

http://identifiers.org/hco/17/GRCh38#69244780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110160572-C-A

69244780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 110160572-C-G

http://identifiers.org/hco/17/GRCh38#69245081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110160804-A-C

http://identifiers.org/hco/17/GRCh38#69245107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110160828-A-C

69245131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110160857-G-A

69245131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110160857-G-C

http://identifiers.org/hco/17/GRCh38#69245200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110160915-C-A

http://identifiers.org/hco/17/GRCh38#69245281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110161009-C-A

69245384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110161129-G-A

http://identifiers.org/hco/17/GRCh38#69245777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110161590-C-A

69246080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110161920-A-T

69246298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162136-C-G

69246304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162141-C-G

69246340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162178-G-T

69246673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162457-A-G

69246758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162548-A-G

69246796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162579-A-T

69246797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162580-G-T

69246814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162597-T-C

http://identifiers.org/hco/17/GRCh38#69246835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110162621-C-A

69246835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162621-C-T

69246952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162735-T-C

69246971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162754-T-C

http://identifiers.org/hco/17/GRCh38#69247034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110162786-A-C

69247034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3 prime UTR variant
orthologous variants: 110162786-A-G

69247153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110162901-G-A

69247153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 110162901-G-T

69247439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 110163164-G-A

69247439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 110163164-G-T

69247512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 110163261-A-G

69247530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 110163278-T-A

69247530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 110163278-T-C

69247552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110163300-A-G

69247558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110163306-T-C

69247649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110163397-G-T

69247664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163412-T-G

69247720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163460-T-C

http://identifiers.org/hco/17/GRCh38#69247726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110163466-A-C

69247726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163466-A-G

69247729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163469-G-T

http://identifiers.org/hco/17/GRCh38#69247732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110163472-A-C

69247732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163472-A-G

69247741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163480-T-C

http://identifiers.org/hco/17/GRCh38#69247778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110163516-A-C

69247792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110163535-T-C

http://identifiers.org/hco/17/GRCh38#69248186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110164081-C-A

69248215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110164110-A-G

69248241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110164131-A-T

69248254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110164144-T-C

69248265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110164155-T-C

69248265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110164155-T-G

69248280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110164170-A-G

69248283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110164173-A-G

69248316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 110164206-A-G

69248342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164231-T-C

http://identifiers.org/hco/17/GRCh38#69248419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110164310-C-A

69248419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164310-C-T

http://identifiers.org/hco/17/GRCh38#69248427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110164318-A-C

69248427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164318-A-T

69248454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164345-T-C

69248476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164368-T-C

69248564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164461-T-C

69248648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164542-T-C

69248658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110164552-T-C

69249724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110165051-T-A

69249724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110165051-T-C

69249724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110165051-T-G

69249988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110165229-G-A

69249988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110165229-G-T

69250005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110165247-T-A

69250005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110165247-T-C

69250031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110165278-T-A

69250031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110165278-T-C

69250053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110165300-A-G

69250070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 110165317-A-G

69250618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110166236-A-G

69250618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 110166236-A-T

69250814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166443-T-G

69250981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166569-G-T

69250984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166572-G-T

69250999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166587-T-C

69251045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166600-G-A

69251048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166603-G-A

69251048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166603-G-T

69251140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166689-G-A

http://identifiers.org/hco/17/GRCh38#69251183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110166724-C-A

69251183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166724-C-G

69251183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166724-C-T

69251186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166727-C-T

69251274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166822-G-T

http://identifiers.org/hco/17/GRCh38#69251278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110166826-C-A

69251349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166886-T-C

69251355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166891-A-T

69251436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110166974-A-G

http://identifiers.org/hco/17/GRCh38#69251531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110167086-C-A

69251531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110167086-C-T

69251541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110167096-A-T

69251687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167220-G-A

69251687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167220-G-T

http://identifiers.org/hco/17/GRCh38#69251886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110167419-C-A

69251926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167462-G-A

69251926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167462-G-T

69251984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167507-T-C

69251984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167507-T-G

http://identifiers.org/hco/17/GRCh38#69252003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110167527-C-A

69252003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110167527-C-T

69253357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168032-C-T

69253540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168175-T-C

69253547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168182-T-C

69253800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110168394-T-C

69253818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110168412-T-G

69253932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168523-G-T

69253946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168537-G-A

69253946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168537-G-T

69253998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168592-G-A

69253998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168592-G-T

69254105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168685-T-C

http://identifiers.org/hco/17/GRCh38#69254194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110168888-A-C

69254194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168888-A-T

http://identifiers.org/hco/17/GRCh38#69254203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110168897-C-A

69254237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168933-T-C

69254291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110168988-G-A

http://identifiers.org/hco/17/GRCh38#69254502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110169184-C-A

69254523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169205-G-A

69254523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169205-G-C

69254523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169205-G-T

http://identifiers.org/hco/17/GRCh38#69254589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110169267-A-C

69254589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169267-A-G

69254733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169277-A-G

69254855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169300-T-C

69254928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169379-G-A

69254928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169379-G-C

69255044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169503-A-G

69255050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169509-T-G

69255197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169619-T-C

69255303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169714-T-A

69255303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169714-T-C

69255303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169714-T-G

69255397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169792-A-G

69255478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169871-A-G

69255482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169876-G-A

69255482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169876-G-T

http://identifiers.org/hco/17/GRCh38#69255510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110169902-A-C

69255510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169902-A-G

69255515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169907-A-G

http://identifiers.org/hco/17/GRCh38#69255534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110169926-A-C

69255534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169926-A-G

69255536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110169928-A-G

69255539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110169931-A-G

69255558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110169950-T-C

69255577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110169969-A-G

69255579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110169971-A-G

69255585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110169977-A-G

69255606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110169998-A-G

69255645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170037-T-A

69255701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170088-A-G

69255866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170251-G-T

69255885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170274-T-A

69255885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170274-T-G

69255972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170346-T-A

69255986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170355-T-C

http://identifiers.org/hco/17/GRCh38#69256068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110170365-C-A

69256087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170382-G-T

69256114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170409-T-A

69256288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110170587-A-G

69256288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110170587-A-T

69256371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170700-G-A

69256371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170700-G-C

69256420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110170748-T-A

69256920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110171099-T-A

69257045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110171231-A-G

69257074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110171262-G-C

69257091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110171279-G-A

69259550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110176358-T-A

http://identifiers.org/hco/17/GRCh38#69259554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110176362-A-C

69259554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110176362-A-T

http://identifiers.org/hco/17/GRCh38#69259556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110176364-C-A

69259557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110176365-T-C

69259693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110176507-A-G

http://identifiers.org/hco/17/GRCh38#69259820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110176634-C-A

69260022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110176913-C-T

69260035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110176925-C-G

69260193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177198-G-T

69260195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177200-T-C

69260253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177250-G-T

69260294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177291-T-C

69260442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177694-G-A

69260442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177694-G-T

http://identifiers.org/hco/17/GRCh38#69260560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110177807-C-A

69260560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110177807-C-G

69260745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178035-A-G

69260763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178053-T-C

http://identifiers.org/hco/17/GRCh38#69260990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110178277-A-C

http://identifiers.org/hco/17/GRCh38#69261075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110178355-C-A

69261075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178355-C-T

69261093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178376-T-C

69261121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178404-T-C

69261155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110178438-T-A

69261316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178609-T-C

69261336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178628-T-C

69261375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178666-G-A

69261375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178666-G-T

http://identifiers.org/hco/17/GRCh38#69261399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110178695-A-C

69261399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178695-A-G

69261399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178695-A-T

69261491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178754-A-T

69261527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178776-T-C

http://identifiers.org/hco/17/GRCh38#69261556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110178805-C-A

69261556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178805-C-T

69261557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178806-A-G

69261589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178842-A-T

69261591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178844-T-A

69261591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178844-T-C

69261626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178880-G-A

69261626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110178880-G-T

69261628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110178882-G-A

69261628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 110178882-G-T

69261686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110178940-G-A

69261686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110178940-G-T

69261719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110178973-T-A

69261719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110178973-T-C

69261764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110179018-A-G

http://identifiers.org/hco/17/GRCh38#69261799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110179040-C-A

69261799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110179040-C-G

http://identifiers.org/hco/17/GRCh38#69261817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110179059-C-A

69261866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110179223-A-G

http://identifiers.org/hco/17/GRCh38#69261907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110179264-A-C

69261969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110179331-C-T

http://identifiers.org/hco/17/GRCh38#69264624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110180502-C-A

69264624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180502-C-T

http://identifiers.org/hco/17/GRCh38#69264641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110180518-C-A

69264641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180518-C-T

69264644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180521-A-T

69264674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180556-T-C

69264674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180556-T-G

69264947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180826-T-C

69264974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180848-T-C

69264974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180848-T-G

69264977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180851-T-C

69264977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110180851-T-G

69265433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110181231-T-C

69265515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110181303-T-C

http://identifiers.org/hco/17/GRCh38#69265560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110181353-C-A

69265627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110181424-G-A

http://identifiers.org/hco/17/GRCh38#69265656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110181453-C-A

69265977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110181701-A-G

69266095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110181821-A-G

69266177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110181917-C-T

http://identifiers.org/hco/17/GRCh38#69267852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110182204-C-A

69267852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110182204-C-T

69267952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110182921-C-G

69267952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110182921-C-T

69268032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110183001-T-A

69268095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183064-T-C

69268101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183070-T-C

69268101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183070-T-G

http://identifiers.org/hco/17/GRCh38#69268144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110183097-A-C

69268144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183097-A-G

69268168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183117-A-T

69268172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183121-G-T

http://identifiers.org/hco/17/GRCh38#69268189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110183132-A-C

69268189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183132-A-G

69268613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110183482-T-C

69268660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183524-A-G

http://identifiers.org/hco/17/GRCh38#69268719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110183647-C-A

http://identifiers.org/hco/17/GRCh38#69268750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110183701-A-C

69268750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 110183701-A-T

http://identifiers.org/hco/17/GRCh38#69268791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110183739-C-A

69268791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 110183739-C-T

69270371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110183918-A-G

http://identifiers.org/hco/17/GRCh38#69270480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110184004-A-C

69270480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184004-A-T

69270584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184041-G-A

69270584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184041-G-T

69270591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184048-A-G

http://identifiers.org/hco/17/GRCh38#69270819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110184270-C-A

69270819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184270-C-T

69271023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184484-T-C

69271098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184554-T-C

http://identifiers.org/hco/17/GRCh38#69271141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110184592-C-A

69271143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184594-T-C

69271144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184595-T-C

http://identifiers.org/hco/17/GRCh38#69271249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110184700-C-A

69271249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110184700-C-T

69271264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 110184715-G-C

69271426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184781-G-T

http://identifiers.org/hco/17/GRCh38#69271482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110184839-C-A

69271523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184874-T-C

69271642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110184987-T-A

69271726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185035-G-A

69271726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185035-G-T

http://identifiers.org/hco/17/GRCh38#69272084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110185282-A-C

69272094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185292-T-C

69272308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185491-A-G

69272319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185527-C-T

69272336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185544-A-G

http://identifiers.org/hco/17/GRCh38#69272595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110185753-A-C

http://identifiers.org/hco/17/GRCh38#69272626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110185784-C-A

69272696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185835-C-T

69272809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110185960-C-T

69272990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186040-G-A

69273183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186215-T-C

69273211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186290-T-C

69273521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186744-T-A

69273601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186823-G-A

69273611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186832-A-G

69273644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186911-C-G

69273644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110186911-C-T

69273755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187091-C-T

69273810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187147-A-G

69273810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187147-A-T

69273840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187170-T-G

http://identifiers.org/hco/17/GRCh38#69273856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110187186-C-A

69273916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187251-G-A

69273916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187251-G-T

http://identifiers.org/hco/17/GRCh38#69273924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110187259-C-A

69273924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187259-C-T

69274153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187484-A-G

http://identifiers.org/hco/17/GRCh38#69274196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110187518-C-A

69274196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110187518-C-T

69276898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188047-T-C

69276979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188123-T-C

69277186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188307-T-C

69277505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188734-G-A

69277505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188734-G-C

69277505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188734-G-T

69277529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188757-G-A

69277529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188757-G-T

69277575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188799-A-G

69277590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188814-T-C

http://identifiers.org/hco/17/GRCh38#69277599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110188823-A-C

69277603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188827-A-G

69277623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188844-G-A

69277623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188844-G-T

69277624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188845-G-C

69277624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110188845-G-T

69277697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110188918-T-C

69277736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110188957-T-C

69277754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 110188975-A-G

http://identifiers.org/hco/17/GRCh38#69277905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110189132-A-C

http://identifiers.org/hco/17/GRCh38#69277926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110189149-A-C

69277926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110189149-A-G

69277926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110189149-A-T

69277963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110189179-T-C

http://identifiers.org/hco/17/GRCh38#69277974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110189190-C-A

http://identifiers.org/hco/17/GRCh38#69283518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110190287-C-A

69283757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110190522-A-G

http://identifiers.org/hco/17/GRCh38#69283810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110190563-A-C

69283844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110190597-T-C

http://identifiers.org/hco/17/GRCh38#69283846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110190599-C-A

69283846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110190599-C-T

http://identifiers.org/hco/17/GRCh38#69283943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110190707-C-A

69283943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110190707-C-G

http://identifiers.org/hco/17/GRCh38#69285682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110192018-A-C

69285682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192018-A-T

69285757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192109-A-T

69285816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192158-G-A

69285816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192158-G-T

http://identifiers.org/hco/17/GRCh38#69285822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110192164-A-C

69285850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192191-A-G

69285965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110192306-A-G

69286338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192674-T-C

69286534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110192828-T-C

69286889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193166-T-C

69287012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193275-C-T

69287155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193414-T-A

69287173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193433-A-T

69287292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193526-G-C

69287469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193699-T-A

69287531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193753-A-G

69287595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110193801-A-G

69287817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194015-G-A

69287817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194015-G-T

69287818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194016-G-A

69287818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194016-G-T

69287822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194020-C-G

69287822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194020-C-T

http://identifiers.org/hco/17/GRCh38#69287978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110194130-A-C

69288044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194188-T-C

69288192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194407-T-A

69288192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194407-T-C

69288284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194491-G-A

69288379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194578-A-G

69289152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194893-A-T

69289165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110194906-A-G

69289334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195076-T-A

69289334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195076-T-C

69289334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195076-T-G

69289346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195088-T-C

http://identifiers.org/hco/17/GRCh38#69289436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110195196-C-A

69289721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195545-T-C

http://identifiers.org/hco/17/GRCh38#69289751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110195570-C-A

69289751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195570-C-T

69289771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195589-G-T

69289814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195629-T-G

69289913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110195727-T-A

69289913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110195727-T-C

69290080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195897-T-C

http://identifiers.org/hco/17/GRCh38#69290095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110195911-C-A

69290136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195951-A-G

69290139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110195954-A-G

http://identifiers.org/hco/17/GRCh38#69290162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110195977-C-A

69290228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196042-C-T

http://identifiers.org/hco/17/GRCh38#69290236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110196050-A-C

69290270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196087-G-A

69290304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196117-A-G

69290582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196402-A-G

69290582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196402-A-T

69290708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196521-C-G

69290862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196679-G-A

69290979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196776-T-A

69290996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196800-A-G

69291156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196966-A-T

69291157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196967-A-G

69291164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196974-T-C

69291166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196976-T-C

69291166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110196976-T-G

69291182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197037-T-A

69291182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197037-T-C

http://identifiers.org/hco/17/GRCh38#69291200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110197053-A-C

69291200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197053-A-G

69291200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197053-A-T

http://identifiers.org/hco/17/GRCh38#69291217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110197072-A-C

69291217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 110197072-A-G

69291223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110197078-A-G

69291232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110197087-G-A

http://identifiers.org/hco/17/GRCh38#69291391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110197245-C-A

69291397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197250-A-G

69291609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197655-A-G

69291638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110197676-G-A

69292360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199016-T-C

69292580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199185-G-A

69292679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199245-C-T

69292720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199301-C-T

69292756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199337-T-C

69292760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199341-T-C

http://identifiers.org/hco/17/GRCh38#69292994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110199587-C-A

69292994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110199587-C-T

69294213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200090-C-T

http://identifiers.org/hco/17/GRCh38#69294589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110200151-C-A

69294589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200151-C-G

69294610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200172-T-C

69294640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200201-A-G

69294693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110200254-G-A

69294693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110200254-G-T

69294724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200285-A-G

http://identifiers.org/hco/17/GRCh38#69294748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110200309-A-C

69294763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200324-T-C

69294773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200327-T-A

69296079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200773-C-T

69296137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200831-T-C

69297172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200945-G-A

69297172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110200945-G-T

69297277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 110201049-T-A

69297328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110201100-A-G

69297383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110201153-T-C

69300829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110201722-T-C

http://identifiers.org/hco/17/GRCh38#69300869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110201752-A-C

69300912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110201798-C-T

http://identifiers.org/hco/17/GRCh38#69301021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110202038-C-A

69301021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202038-C-G

69301021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202038-C-T

69301025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202042-G-A

69301025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202042-G-C

69301025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202042-G-T

69301073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202081-G-T

69301111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202119-A-G

69301146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110202144-G-T

69301296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202302-A-G

http://identifiers.org/hco/17/GRCh38#69301342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110202345-C-A

69301342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202345-C-T

http://identifiers.org/hco/17/GRCh38#69301372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110202374-C-A

69301404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202428-T-C

http://identifiers.org/hco/17/GRCh38#69301414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110202474-A-C

69301414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202474-A-T

69301503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202783-T-C

69301601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202882-T-A

69301669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202921-G-A

69301729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110202977-A-T

69301782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110203022-G-A

69301823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110203062-T-C

69302103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110203337-A-G

69302180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110203408-T-G

69302462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 110203867-C-T

69302814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 110204251-A-G

69302940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110204375-T-C

69303027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110204444-A-G

69303027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110204444-A-T

69303031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110204456-T-A

69303056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110204481-A-G

69304099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110204818-T-C

69304149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110204868-T-A

69304482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110205174-T-C

69304482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110205174-T-G

69304519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110205212-G-A

69304519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110205212-G-T

http://identifiers.org/hco/17/GRCh38#69304520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110205213-C-A

69304520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110205213-C-T

69304687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110205368-G-A

69304789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110205470-A-G

69304938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110205597-G-T

http://identifiers.org/hco/17/GRCh38#69304951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110205610-C-A

69305156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110205806-G-A

69305336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110205981-A-T

69306271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208155-A-G

69306354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208240-G-T

http://identifiers.org/hco/17/GRCh38#69306578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110208387-C-A

69306618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208426-G-A

69306618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208426-G-C

69306618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208426-G-T

69306671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208476-G-A

69306671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208476-G-T

69306673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208478-A-G

69306681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208486-T-A

69306681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208486-T-C

69306685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208490-A-T

69306713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208518-T-C

69306775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110208578-T-C

69306793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110208596-G-A

69306793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110208596-G-T

69306862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110208665-G-C

69306916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110208719-T-C

69306946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110208749-G-A

69306951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: missense variant
orthologous variants: 110208754-T-C

http://identifiers.org/hco/17/GRCh38#69306977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110208780-C-A

69306993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208791-T-C

69307018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208816-G-A

69307018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110208816-G-T

69307243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110209027-T-C

http://identifiers.org/hco/17/GRCh38#69307326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110209100-A-C

69307629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110209889-C-G

69307642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110209902-T-A

69307642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110209902-T-C

69307668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110209932-C-T

69307805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210074-C-G

69308233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210581-A-G

69308243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210591-G-T

69308252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210593-T-A

69308252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210593-T-C

69308255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210596-G-A

69308255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210596-G-T

69308325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110210665-T-C

69308372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110210712-T-A

69308372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110210712-T-C

69308372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 110210712-T-G

http://identifiers.org/hco/17/GRCh38#69308408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110210748-C-A

69308408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210748-C-T

http://identifiers.org/hco/17/GRCh38#69308418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110210759-C-A

69308439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210779-T-C

69308440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210780-G-A

69308440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210780-G-T

69308462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210798-T-A

69308462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210798-T-C

69308478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210814-T-A

69308478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210814-T-C

http://identifiers.org/hco/17/GRCh38#69308486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110210823-C-A

69308486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210823-C-T

69308549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110210880-T-C

http://identifiers.org/hco/17/GRCh38#69308682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110216681-C-A

69308721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110216716-A-T

69308855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110216842-C-T

69309060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217088-A-G

69309063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217091-T-C

69309154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217293-G-T

69309162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217301-G-A

69309162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217301-G-C

69309162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217301-G-T

69309180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217319-C-T

69309287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110217411-T-C

69309305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110217429-A-G

69309380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110217504-T-C

69309403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: missense variant
orthologous variants: 110217527-T-C

69309442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217566-A-G

69309445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217569-T-A

69309445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110217569-T-C

69310082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218003-A-T

http://identifiers.org/hco/17/GRCh38#69310104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110218018-C-A

69310591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218246-T-C

69310636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218290-C-T

69310765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218336-G-A

69310765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218336-G-C

69313034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218503-G-A

69313034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218503-G-C

69313034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218503-G-T

69313067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218533-G-T

69313111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110218577-A-G

http://identifiers.org/hco/17/GRCh38#69313153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110218619-A-C

69313174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: 110218640-A-T

http://identifiers.org/hco/17/GRCh38#69313288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110218754-A-C

http://identifiers.org/hco/17/GRCh38#69313339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110218806-C-A

69313339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218806-C-T

69313341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218808-G-A

69313341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218808-G-T

http://identifiers.org/hco/17/GRCh38#69313439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110218900-C-A

69313439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110218900-C-T

69313565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219038-T-C

http://identifiers.org/hco/17/GRCh38#69313694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110219348-A-C

69313795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219453-C-T

69313879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219523-C-G

69313909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219548-T-C

69313921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219560-G-T

69313924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219563-C-T

69313940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219579-T-C

69313940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219579-T-G

69314027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219651-T-C

69314098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219729-A-G

69314115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219746-T-A

69314141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219767-T-G

69314183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219802-T-A

69314214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219838-T-C

69314238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219858-A-G

69314238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron variant
orthologous variants: 110219858-A-T

http://identifiers.org/hco/17/GRCh38#69314462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220105-C-A

69314462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220105-C-G

69314462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220105-C-T

http://identifiers.org/hco/17/GRCh38#69314472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220122-C-A

69314472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220122-C-T

69314474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220124-G-A

69314474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220124-G-C

69314483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220133-A-G

69314486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220136-T-A

69314492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220142-T-C

http://identifiers.org/hco/17/GRCh38#69314505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220154-A-C

69314507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220156-G-A

69314513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220162-G-A

69314513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220162-G-T

http://identifiers.org/hco/17/GRCh38#69314545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220196-C-A

69314560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220211-C-T

69314561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220212-T-A

69314561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220212-T-C

http://identifiers.org/hco/17/GRCh38#69314581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220228-C-A

http://identifiers.org/hco/17/GRCh38#69314655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220303-C-A

69314676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220330-T-C

http://identifiers.org/hco/17/GRCh38#69314692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220346-C-A

69314746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220448-G-C

http://identifiers.org/hco/17/GRCh38#69314747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220449-A-C

69314747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220449-A-T

69314752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220454-G-A

69314752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220454-G-T

69314769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220605-G-T

69314776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220612-G-A

69314776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220612-G-C

http://identifiers.org/hco/17/GRCh38#69314827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220664-C-A

69314827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220664-C-G

69314834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220671-G-A

69314834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220671-G-C

69314847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220684-T-A

69314847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220684-T-C

69314910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220746-C-T

69314950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220785-G-A

69314952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220787-G-T

69315036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220882-A-G

http://identifiers.org/hco/17/GRCh38#69315056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220887-C-A

69315056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220887-C-T

http://identifiers.org/hco/17/GRCh38#69315135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110220964-A-C

69315135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 110220964-A-G

69319210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110222980-C-T

69319482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110223234-C-T

69319619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110223541-A-G

69319825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110223926-A-G

69320099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110224194-C-T

69320189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110224285-G-A

69320219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110224315-A-T

69320261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110224350-A-T

69320478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110224572-C-T

69320533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110224632-A-G

69322837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225245-T-C

69323780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225662-T-C

69323825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225710-A-G

69323849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225734-C-T

69323854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225772-G-A

69323975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225967-T-C

69323975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110225967-T-G

http://identifiers.org/hco/17/GRCh38#69324183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110226180-A-C

69324218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110226215-T-C

http://identifiers.org/hco/17/GRCh38#69324307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110226299-A-C

69324390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110226382-A-G

69324487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110226476-C-T

69324663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110226630-C-G

69324701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110226670-T-A

69325940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110227417-C-T

69326077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110227546-A-T

69326134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110227608-T-G

69326377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110227801-C-T

69326412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110227836-T-A

69326720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110228151-C-G

69326747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110228177-A-G

http://identifiers.org/hco/17/GRCh38#69326768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228196-C-A

69326915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110228285-A-G

http://identifiers.org/hco/17/GRCh38#69326916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228286-C-A

69326916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110228286-C-T

http://identifiers.org/hco/17/GRCh38#69326973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228303-C-A

69326987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110228315-T-C

http://identifiers.org/hco/17/GRCh38#69327031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228356-C-A

69327031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110228356-C-T

http://identifiers.org/hco/17/GRCh38#69327054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228375-C-A

69327054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 110228375-C-G

69327054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 110228375-C-T

69327190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 110228541-C-G

http://identifiers.org/hco/17/GRCh38#69327209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228562-C-A

http://identifiers.org/hco/17/GRCh38#69327218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110228571-C-A

69327218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 110228571-C-G

69327218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 35
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 110228571-C-T