73694445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78521305-C-T

73694588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78521443-C-T

73695144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78521973-A-G

http://identifiers.org/hco/6/GRCh38#73695565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78522515-A-C

73695565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78522515-A-G

73695624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522570-T-C

73695688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78522632-G-A

73695688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78522632-G-T

73695694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78522638-G-T

http://identifiers.org/hco/6/GRCh38#73695776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78522738-C-A

73695776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522738-C-G

73695776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522738-C-T

73695817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78522778-G-A

73695817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78522778-G-T

73695823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78522784-T-G

http://identifiers.org/hco/6/GRCh38#73695877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78522839-C-A

73695882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78522844-G-A

73695899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522860-G-A

http://identifiers.org/hco/6/GRCh38#73695904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#78522865-C-A

73695904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522865-C-G

73695904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522865-C-T

73695920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522881-G-A

73695920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522881-G-T

73695937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522899-G-A

73695937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78522899-G-T

73695977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78522940-T-C

73695977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78522940-T-G

http://identifiers.org/hco/6/GRCh38#73696088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523044-C-A

73696088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 78523044-C-T

http://identifiers.org/hco/6/GRCh38#73696128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523084-A-C

73696140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523096-G-T

73696150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78523106-G-A

73696150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78523106-G-C

73696150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78523106-G-T

http://identifiers.org/hco/6/GRCh38#73696168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523122-C-A

73696168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523122-C-T

73696200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523151-G-A

73696200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523151-G-C

73696200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523151-G-T

73696207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523158-G-A

73696207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523158-G-T

http://identifiers.org/hco/6/GRCh38#73696208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523159-C-A

73696208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523159-C-T

http://identifiers.org/hco/6/GRCh38#73696209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523160-C-A

73696209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523160-C-G

73696209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78523160-C-T

73696222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant
orthologous variants: 78523170-G-A

73696222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant
orthologous variants: 78523170-G-C

73696222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant
orthologous variants: 78523170-G-T

http://identifiers.org/hco/6/GRCh38#73696269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523217-C-A

73696269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 78523217-C-G

73696269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 78523217-C-T

73696270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant
orthologous variants: 78523218-G-A

73696270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant
orthologous variants: 78523218-G-C

73696270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant
orthologous variants: 78523218-G-T

http://identifiers.org/hco/6/GRCh38#73696314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#78523256-C-A

73696314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78523256-C-G

73696314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78523256-C-T

73696392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78523281-G-A

73696581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78523374-C-T

73696935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78523806-C-T

73697105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78523946-A-G

73697609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78524358-T-C

73697614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78524363-A-G

http://identifiers.org/hco/6/GRCh38#73697662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78524411-C-A

73698268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525046-T-C

73698296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525062-C-T

73698643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525418-A-G

73698745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525522-T-C

73698747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525524-G-A

73698809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525582-A-G

http://identifiers.org/hco/6/GRCh38#73699033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78525945-C-A

73699033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78525945-C-G

73699184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78526095-C-T

73699700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78526618-G-A

http://identifiers.org/hco/6/GRCh38#73699849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78526746-A-C

73699900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78526794-T-G

http://identifiers.org/hco/6/GRCh38#73700824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78527460-C-A

73701133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78527692-A-G

73701133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78527692-A-T

73701134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78527693-T-G

73701612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78527963-C-T

73701643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78527973-C-G

73701777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78528108-C-G

73701937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78528316-T-A

73701938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78528317-T-C

http://identifiers.org/hco/6/GRCh38#73701961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78528328-C-A

http://identifiers.org/hco/6/GRCh38#73702064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78528501-A-C

73702064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78528501-A-G

73702149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78528591-C-G

73702266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78528925-A-G

73702691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78529302-G-A

73702847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78529649-G-A

73702934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78529736-A-G

73703101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78529870-G-T

73703183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78529949-T-A

73703788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78530503-C-T

73703820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78530535-T-C

73703820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78530535-T-G

73703869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78530582-C-T

http://identifiers.org/hco/6/GRCh38#73703935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78530647-A-C

73704530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78530934-A-G

73704532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78530936-G-A

73704551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78530952-A-G

73704644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78531045-C-T

73704656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78531057-G-T

73704723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78531118-A-G

73704837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78531199-G-C

73704909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78532249-A-G

73705107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78532466-A-G

http://identifiers.org/hco/6/GRCh38#73705278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78532616-A-C

73706264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78533048-G-A

73706394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78533171-A-G

73706408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78533185-G-A

73706472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78533244-C-T

73706549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78533366-G-A

73707849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78534621-G-A

73710816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, undefined
orthologous variants: 78535119-G-A

73711073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535318-C-G

73711153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535388-G-A

73712387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535831-C-T

73712414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535858-A-G

73712470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535912-T-G

73712475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535917-T-C

73712483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535925-T-C

73712507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78535948-G-T

73712631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536058-A-T

73712963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536358-G-A

73713099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536484-C-T

73713120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536505-T-G

73713177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536561-A-G

73713305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536694-G-T

73713351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536736-A-G

73713361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536745-G-A

http://identifiers.org/hco/6/GRCh38#73713501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78536779-C-A

73713661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536871-A-G

73713672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536882-G-A

73713748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78536968-C-T

73713813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78537019-C-T

73713897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78537101-G-T

73714140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78537345-C-T

73714153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78537358-T-C

73714236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78537435-C-T

73719905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539433-T-C

73719914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539442-A-G

73719938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539463-G-A

73719984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539487-G-A

73720009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539511-A-T

73720043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539543-C-T

73720146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539644-G-A

73720441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539862-A-G

73720519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539939-G-A

73720519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539939-G-C

73720541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78539963-A-G

73720744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540071-A-G

73720848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540113-G-A

73720848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540113-G-T

73720963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540196-C-T

73720971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540204-T-C

73720977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540210-G-A

73721221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540414-T-A

http://identifiers.org/hco/6/GRCh38#73721270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78540461-A-C

73721270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540461-A-T

73721272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540463-T-C

73722084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78540780-A-G

73722350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 78541022-A-G

73722504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78541181-A-G

73722657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78541278-T-G

73722746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78541365-A-G

73722913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 78541579-C-T

73723018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78541739-T-G

http://identifiers.org/hco/6/GRCh38#73723276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78541954-A-C

73723310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78541993-G-A

73723310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78541993-G-T

73723408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542299-G-A

73723408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542299-G-C

73723408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542299-G-T

73729886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543166-C-T

73729918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543198-A-G

73729999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543271-G-A

73730089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543462-G-A

73730099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543472-C-T

73730203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543582-A-T

73730211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543590-G-A

73730211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543590-G-C

73730211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543590-G-T

73730230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543612-T-A

73730230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543612-T-C

73730236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543618-T-G

73730302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543689-A-G

73730309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543696-T-G

http://identifiers.org/hco/6/GRCh38#73730339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78543726-C-A

73730339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78543726-C-T

73730388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78543775-C-T

http://identifiers.org/hco/6/GRCh38#73730553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78543940-C-A

73730553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78543940-C-T

73730602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543989-G-C

73730602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543989-G-T

73730636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544023-G-T

73730645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544032-G-A

73730645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544032-G-T

73730761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544119-A-G

73730771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544129-T-A

73730772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544130-G-A

73730908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544252-G-T

73730928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544275-A-G

73732969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544798-G-T

http://identifiers.org/hco/6/GRCh38#73733153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78544959-A-C

73733153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544959-A-G

73733179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544982-G-A

73733296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545029-G-A

73733479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545161-C-T

73733628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545295-G-T

73734252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545453-C-T

http://identifiers.org/hco/6/GRCh38#73734266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78545467-C-A

73734432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545647-T-C

73734433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545648-A-G

73734478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545692-A-G

73734794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545996-T-G

73735123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546279-G-A

73735439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546602-A-G

73735454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546614-G-A

73735683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546812-T-G

73735748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546877-G-A

73735765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546900-G-A

73735794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546929-C-T

73735988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548630-A-G

73735998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548640-G-C

73736044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548686-G-T

http://identifiers.org/hco/6/GRCh38#73736249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78549116-C-A

73736249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549116-C-T

73736257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549124-G-T

73736258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549125-T-C

73736269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549136-G-A

73736269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549136-G-C

73736269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549136-G-T

http://identifiers.org/hco/6/GRCh38#73736308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78549189-A-C

73736308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549189-A-G

73736308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549189-A-T

73736315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549196-C-T

http://identifiers.org/hco/6/GRCh38#73736334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78549211-A-C

73736334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549211-A-G

http://identifiers.org/hco/6/GRCh38#73736584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78549462-C-A

73736584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549462-C-T

http://identifiers.org/hco/6/GRCh38#73736636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78549509-C-A

73736636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549509-C-G

73736636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549509-C-T

73736644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549517-T-G

73736709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549556-A-G

73736711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549558-T-C

73736736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549583-T-G

73736816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549676-G-C

73736941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549799-T-C

73737156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552305-T-C

http://identifiers.org/hco/6/GRCh38#73737254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78552398-A-C

73737336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552463-T-C

73737350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552476-C-T

73737371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552497-C-G

73737532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552645-T-C

73737551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552659-A-G

73739210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553351-A-G

73739320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553511-T-G

http://identifiers.org/hco/6/GRCh38#73740301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78553858-C-A

http://identifiers.org/hco/6/GRCh38#73740319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78553874-A-C

73740387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553938-G-A

73747299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555820-C-G

73747358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555877-T-C

73747504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555964-C-T

73747608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556062-C-G

73747746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556124-A-G

73748187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556306-A-G

http://identifiers.org/hco/6/GRCh38#73748258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78556369-C-A

http://identifiers.org/hco/6/GRCh38#73748568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78556653-A-C

http://identifiers.org/hco/6/GRCh38#73748582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78556673-C-A

73748582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556673-C-T

73748726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556812-G-A

73753870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

73753957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

73754137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

73754178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

73755229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558951-T-C

73756040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561221-G-A

73756199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561375-A-G

http://identifiers.org/hco/6/GRCh38#73756570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78561788-C-A

73756570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561788-C-T

http://identifiers.org/hco/6/GRCh38#73756734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78561933-C-A

73756734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561933-C-T

73756770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561967-G-A

73756770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78561967-G-T

73756947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78562124-C-T

http://identifiers.org/hco/6/GRCh38#73757110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78562730-A-C

73757616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563256-A-G

73757816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563449-G-A

73757974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563598-G-A

73758350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563973-A-G

73758765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564596-T-C

73758790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564617-G-A

http://identifiers.org/hco/6/GRCh38#73758793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78564620-C-A

73758793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564620-C-T

http://identifiers.org/hco/6/GRCh38#73758815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78564642-C-A

73758815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564642-C-G

73758816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564643-C-T

http://identifiers.org/hco/6/GRCh38#73758843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78564669-A-C

73758843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564669-A-T

73758867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564693-T-C

73758869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564695-G-T

73759002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78564785-G-A

73759078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564861-G-T

73759094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564882-T-C

73759096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564884-T-C

73759101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564889-T-C

73759127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564917-T-A

73759127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564917-T-C

73759155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564946-G-T

73759297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565059-G-T

73759806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565333-G-C

http://identifiers.org/hco/6/GRCh38#73761208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78566927-A-C

73761409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567130-T-C

73761410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567131-T-C

73761511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567227-A-G

73762222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567344-A-G

73762275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567387-A-T

73762327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567480-T-C

73762417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78567578-A-G

73762438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78567599-A-T

73762441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78567602-C-T

73762512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567673-T-C

73762659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568086-T-C

73762659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568086-T-G

73762729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568162-T-C

http://identifiers.org/hco/6/GRCh38#73762803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78568254-A-C

73762803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78568254-A-G

73762818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78568269-A-G

73762820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78568271-A-G

73762820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78568271-A-T

73762830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78568281-A-G

73762845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78568296-A-G

73762942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568366-T-A

http://identifiers.org/hco/6/GRCh38#73763435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78568807-C-A

73763439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568811-G-T

73763462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568834-G-T

73763494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568866-G-T

73763520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568879-G-C

73763520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568879-G-T

73763549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568908-T-C

http://identifiers.org/hco/6/GRCh38#73763784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78569127-C-A

73763784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569127-C-G

73763794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569137-A-G

73763794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569137-A-T

73763797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569144-A-T

73763818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569165-G-T

http://identifiers.org/hco/6/GRCh38#73763822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78569166-C-A

73763822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569166-C-T

http://identifiers.org/hco/6/GRCh38#73763823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78569167-A-C

73763823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569167-A-G

73763827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569171-A-G

73765135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570055-T-C

http://identifiers.org/hco/6/GRCh38#73765181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78570096-C-A

73765409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570569-G-A

73765431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570593-T-C

73765582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570726-A-G

73765730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571277-A-G

73765779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571324-T-C

73765826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571370-A-G

73765835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571379-G-A

73765835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571379-G-C

http://identifiers.org/hco/6/GRCh38#73765861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78571405-C-A

73765861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571405-C-G

73766110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78571656-A-G

73766139-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78571685-T-G

73766187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571726-A-G

73766255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571794-G-T

73766285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78571819-A-G

73766285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78571819-A-T

73766300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571835-G-A

73766300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571835-G-T

73766607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572583-T-A

73766607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572583-T-C

73766644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572617-G-T

http://identifiers.org/hco/6/GRCh38#73766718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78572687-C-A

73766718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572687-C-T

http://identifiers.org/hco/6/GRCh38#73766763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78572730-A-C

73766763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78572730-A-G

73766763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78572730-A-T

73766905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572872-T-C

73766916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572883-A-G

73766937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572907-T-G

73767064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573012-T-A

73767422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573234-A-G

73767633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573387-G-A

73767633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573387-G-T

73767791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573541-G-A

73767953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574402-T-C

http://identifiers.org/hco/6/GRCh38#73767974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78574417-A-C

73767974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574417-A-G

73768038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574505-T-C

73768154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78574620-G-A

73768177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78574643-G-A

73768265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574726-C-T

http://identifiers.org/hco/6/GRCh38#73768322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78574783-C-A

73768706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575128-G-A

73769534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576323-T-A

73769543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576332-A-G

73769543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576332-A-T

73771229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576811-G-A

73771608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577164-A-G

73771665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577209-G-A

73771665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577209-G-C

73771665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78577209-G-T

73779343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578010-G-C

73779634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578250-C-T

73779929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578730-A-G

73779966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578767-T-C

73779986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578787-A-T

73780048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578817-G-A

73780048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578817-G-T

73780049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578818-A-T

73780059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578828-G-T

73780163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78578925-T-C

73780191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78578955-C-G

73780231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 78578995-A-G

http://identifiers.org/hco/6/GRCh38#73780294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78579059-C-A

http://identifiers.org/hco/6/GRCh38#73780301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78579066-C-A

73780301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579066-C-T

73780335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579100-T-G

73780348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579110-T-C

73780355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579116-A-G

73780363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579124-G-T

73780370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579131-G-A

73780373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579139-T-C

73780386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579157-T-C

73780389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579160-A-G

73780402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579171-G-A

73780629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579385-A-T

73780717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579474-A-G

73781113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579716-G-A

73781117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579720-G-A

73781117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579720-G-T

73781127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579730-A-G

http://identifiers.org/hco/6/GRCh38#73781137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78579740-A-C

73781137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579740-A-T

http://identifiers.org/hco/6/GRCh38#73781330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78579905-C-A

73781330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579905-C-T

73781352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579929-T-A

73781362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579967-G-T

73781363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579968-A-G

73781489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580069-A-G

73782285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580366-A-G

73782552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587240-G-T

73782582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587272-T-G

73782602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587292-G-A

73782636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78587325-G-A

73782645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78587334-G-A

73782716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78587405-A-G

73782789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587482-T-G

73782831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587524-A-G

73782841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587537-T-A

73782844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587540-A-G

73782855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587551-A-G

73782861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587557-G-T

73782863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587559-A-T

http://identifiers.org/hco/6/GRCh38#73782873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78587569-C-A

73782873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587569-C-G

73782873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587569-C-T

73782880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587576-G-A

73782880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587576-G-T

73782901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587598-T-A

73782901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587598-T-G

73783013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587703-C-G

73783404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587841-T-G

http://identifiers.org/hco/6/GRCh38#73783606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78587989-A-C

73783606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587989-A-G

73783626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78588009-A-G

73783644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78588025-G-A

73783644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78588025-G-T

73783676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78588057-G-T

73783699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78588077-G-A

73783699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78588077-G-C

73783699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78588077-G-T

73783746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78588124-T-C

73784239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590894-T-C

73784452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78591111-T-A

73784516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78591286-C-T

73784914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78591717-A-G

73785291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592044-A-T

73785294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592047-G-A

73785294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592047-G-T

73785307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592056-T-C

73785447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78592200-T-C

http://identifiers.org/hco/6/GRCh38#73785453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78592206-C-A

73785481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592234-A-G

73785537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592287-A-G

73785540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592290-G-A

73785540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592290-G-T

73785586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593226-A-G

73785586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593226-A-T

73785603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593243-T-A

73785603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593243-T-C

73785603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593243-T-G

73785673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593315-C-T

73785750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593389-T-C

73786161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594143-T-C

73786195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594207-C-T

73786248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594264-C-T

73786605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594627-A-T

73786709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594720-G-T

73786870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595733-T-C

http://identifiers.org/hco/6/GRCh38#73786940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78595802-C-A

73786987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595843-G-A

73787174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595940-A-G

73787338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78596116-T-G

73787342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78596120-G-A

http://identifiers.org/hco/6/GRCh38#73787491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78596273-C-A

73787491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596273-C-T

73787598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596364-T-G

73787599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596365-G-T

73787988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596755-C-T

http://identifiers.org/hco/6/GRCh38#73788367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78596896-C-A

73788367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596896-C-G

http://identifiers.org/hco/6/GRCh38#73788378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78596907-C-A

73788378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596907-C-T

73788416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596945-C-T

73788448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596973-G-T

73788643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597161-T-C

73788685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597201-A-G

73788685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597201-A-T

73788924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597618-T-C

73789032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597767-T-A

73789277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597995-C-T

73789284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598001-G-A

73792543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598389-G-A

73792543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598389-G-C

73792543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598389-G-T

73792622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78598467-C-G

http://identifiers.org/hco/6/GRCh38#73792780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78598625-A-C

73792780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78598625-A-G

http://identifiers.org/hco/6/GRCh38#73792819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78598668-C-A

73792819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598668-C-G

73792819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598668-C-T

http://identifiers.org/hco/6/GRCh38#73792831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78598679-C-A

73792831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598679-C-T

73792835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598683-G-A

73792835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598683-G-T

73792892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598744-G-A

73792892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598744-G-C

73792925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598782-G-A

73793136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598921-G-A

73793153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598929-G-C

http://identifiers.org/hco/6/GRCh38#73793280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78598987-C-A

73793345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599016-T-C

73793351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599022-C-T

73793623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599249-C-T

73793886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599464-T-C

73796676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600112-G-C

73796771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600206-G-T

73797125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600453-G-A

73797125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600453-G-T

73797758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601054-C-T

73797803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601099-T-C

73797836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601135-G-T

73797957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601256-G-A

73798508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601502-T-C

73798521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601515-C-T

73798536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601530-C-G

73798670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78601648-T-C

73798694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78601675-G-C

http://identifiers.org/hco/6/GRCh38#73798738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#78601721-A-C

73802219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602633-T-C

73802287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602701-G-A

73802298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602712-T-C

73802299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602713-A-G

73802299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602713-A-T

73802364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602746-T-C

73802466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602845-G-A

73802599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602962-A-G

73803132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603042-T-A

73803138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603046-C-G

73803138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603046-C-T

73803180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603068-T-C

73803230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78603112-A-G

73803269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78603151-T-C

73803281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 78603163-T-A

73803281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78603163-T-C

73803281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 78603163-T-G

http://identifiers.org/hco/6/GRCh38#73803330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78603219-C-A

73803330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603219-C-T

http://identifiers.org/hco/6/GRCh38#73803369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78603258-C-A

73803369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603258-C-G

73803369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603258-C-T

http://identifiers.org/hco/6/GRCh38#73803385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78603278-A-C

73803385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603278-A-G

http://identifiers.org/hco/6/GRCh38#73803414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78603300-C-A

73803544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78603412-G-T

73803607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78603468-C-T

73803801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78603641-C-T

73806591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605141-A-G

73806592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605142-G-C

http://identifiers.org/hco/6/GRCh38#73806707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78605240-C-A

73806707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605240-C-T

http://identifiers.org/hco/6/GRCh38#73806715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78605248-C-A

73806715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605248-C-T

73806748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605278-T-C

73806807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605329-A-T

73807306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605798-A-G

73807339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605830-A-G

73807414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605883-C-T

73807432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605894-G-C

73807521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606094-G-A

73807527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606100-G-A

73807758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607156-A-G

73807960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607370-A-G

73808013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607422-G-T

73808021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607430-T-C

73808021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607430-T-G

73808263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607657-C-G

73808269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607663-G-C

73808326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607721-T-C

73808371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607782-T-A

73808371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607782-T-C

73808883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78608423-G-T

73809011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609631-C-T

73809044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609662-G-T

73809847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610189-A-G

73809935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610273-G-A

73809935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610273-G-C

73809942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610280-T-C

73810054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78610388-T-G

73810060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78610394-T-G

73810177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78610508-G-A

73810181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 78610512-G-A

73810868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78610786-A-T

http://identifiers.org/hco/6/GRCh38#73810871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78610789-C-A

73810881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78610799-T-C

73810888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78610806-T-A

73810944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78610868-G-A

73810956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78610880-T-C

http://identifiers.org/hco/6/GRCh38#73810983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78610926-C-A

http://identifiers.org/hco/6/GRCh38#73811173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78611114-A-C

73811192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78611133-T-C

73811214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78611155-T-C

73811570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78611487-T-C

73811587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78611504-C-G

73811650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78611563-G-C

73811693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78611629-T-C

73811942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612066-A-T

73811953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612077-G-A

73812031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612143-A-G

http://identifiers.org/hco/6/GRCh38#73812078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612190-C-A

73812078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612190-C-T

http://identifiers.org/hco/6/GRCh38#73812105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612217-C-A

73812105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612217-C-G

73812105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612217-C-T

73812106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612218-T-G

73812127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612239-G-A

73812127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612239-G-T

73812167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612279-A-G

http://identifiers.org/hco/6/GRCh38#73812173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612285-A-C

73812173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612285-A-G

73812173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612285-A-T

http://identifiers.org/hco/6/GRCh38#73812209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612324-C-A

73812303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612421-T-C

http://identifiers.org/hco/6/GRCh38#73812373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612485-A-C

73813213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612923-A-G

http://identifiers.org/hco/6/GRCh38#73813238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612948-A-C

73813258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78612965-C-G

http://identifiers.org/hco/6/GRCh38#73813279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78612991-A-C

73813323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613031-T-C

73813342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613049-G-A

73813342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613049-G-T

http://identifiers.org/hco/6/GRCh38#73813467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78613142-C-A

73813476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613151-C-T

73813566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613238-G-C

73813566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613238-G-T

73813597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613269-C-G

73813712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613379-A-G

73813767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613431-T-C

73814010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613677-A-G

http://identifiers.org/hco/6/GRCh38#73814011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78613678-A-C

73814111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613760-T-C

73814121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613770-T-A

73814121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613770-T-C

73814147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613796-T-G

73814181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613815-C-T

73814182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613816-G-A

73814182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613816-G-T

73814279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613908-T-C

73814280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78613909-G-A

http://identifiers.org/hco/6/GRCh38#73814294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78613922-A-C

73814422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614047-C-T

73814433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614058-G-T

73814461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614090-A-G

73814511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614140-A-G

73814833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614492-G-A

73814833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614492-G-T

http://identifiers.org/hco/6/GRCh38#73814834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78614493-C-A

73814834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614493-C-T

73814919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614573-A-G

73814940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614639-T-C

73814940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614639-T-G

73814973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 78614718-T-C

73814998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: synonymous variant
orthologous variants: 78614743-T-C

http://identifiers.org/hco/6/GRCh38#73815037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78614782-C-A

73815037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: synonymous variant
orthologous variants: 78614782-C-T

73815088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense variant
orthologous variants: 78614830-T-G

http://identifiers.org/hco/6/GRCh38#73815157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78614887-C-A

73815157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614887-C-T

73815187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614916-A-G

73815187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614916-A-T

73815215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614948-G-A

73815215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614948-G-C

73815215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614948-G-T

73815230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78614961-G-T

73815272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78615002-A-G

http://identifiers.org/hco/6/GRCh38#73815308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78615037-C-A

http://identifiers.org/hco/6/GRCh38#73815558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78616099-A-C

73815558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616099-A-T

73815691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616215-G-A

73815691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616215-G-C

73815745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616250-T-C

73815816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616324-G-A

73816062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616547-C-T

73816173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616630-C-T

73816174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78616631-C-T

73818076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617118-G-A

73818076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617118-G-T

73818081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617123-T-C

73818093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617135-A-G

73818100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617142-A-G

73818104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617147-T-C

73818144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617186-G-T

73818182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617218-A-G

73818216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617252-C-T

73818274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617304-T-G

73818330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617360-G-A

http://identifiers.org/hco/6/GRCh38#73818569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78617600-A-C

73818569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78617600-A-G

73818796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78618173-A-G

73820034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619389-T-C

73820038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619393-C-T

73820051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619406-C-T

73820152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619494-G-A

73820163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619505-C-G

73820163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619505-C-T

73820182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619523-T-C

73820226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619559-A-T

73820312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619647-A-G

73820315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619650-A-G

http://identifiers.org/hco/6/GRCh38#73820333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78619669-C-A

73820347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619683-T-C

http://identifiers.org/hco/6/GRCh38#73820349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78619685-C-A

73820349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619685-C-T

73820394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619732-A-G

73820395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619733-A-G

73820398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619736-G-T

73820401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619739-T-C

http://identifiers.org/hco/6/GRCh38#73820455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78619813-C-A

73820542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense variant
orthologous variants: 78619900-A-G

73820585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619942-T-A

73820585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619942-T-C

73820608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619965-G-A

http://identifiers.org/hco/6/GRCh38#73820633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78619987-C-A

73820633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619987-C-T

73820639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78619993-A-G

73820682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620034-G-A

73820682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620034-G-C

73820682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620034-G-T

73820704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620056-A-G

73820704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620056-A-T

73820705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620057-A-G

73820705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620057-A-T

73820733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620083-T-C

73820787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620140-A-G

73820836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620200-T-C

73820837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620201-A-G

73821984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620345-C-G

73822126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620482-G-A

73822133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620489-T-C

73822297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620648-T-C

73822308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620659-G-A

73822352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620703-C-T

73822575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620937-C-T

73822637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620999-G-A

73822637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78620999-G-T

http://identifiers.org/hco/6/GRCh38#73822674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78621208-A-C

73823158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78621912-C-T

73823233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78621969-A-G

73823307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78622038-T-A

73823307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78622038-T-C

73823348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78622079-G-T

73823353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78622084-G-T

73823389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78622107-T-C

http://identifiers.org/hco/6/GRCh38#73823426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622143-C-A

73823426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: intron variant
orthologous variants: 78622143-C-T

73823557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: stop gained
orthologous variants: 78622270-C-G

73823563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense variant
orthologous variants: 78622276-C-G

73823563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: missense variant
orthologous variants: 78622276-C-T

73823703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622417-G-A

73823703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622417-G-T

http://identifiers.org/hco/6/GRCh38#73823746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622464-C-A

73823746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622464-C-T

http://identifiers.org/hco/6/GRCh38#73823795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622509-C-A

73823811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622525-T-G

73823843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622559-G-C

73823843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622559-G-T

73823846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622562-G-T

http://identifiers.org/hco/6/GRCh38#73823864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622580-C-A

73823864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622580-C-G

73824041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622725-G-A

73824041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622725-G-C

73824041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622725-G-T

http://identifiers.org/hco/6/GRCh38#73824042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622726-C-A

73824042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622726-C-T

http://identifiers.org/hco/6/GRCh38#73824067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622753-C-A

73824127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622795-T-C

http://identifiers.org/hco/6/GRCh38#73824223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78622891-C-A

73824223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622891-C-G

73824325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78622975-C-T

http://identifiers.org/hco/6/GRCh38#73824378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78623027-C-A

73824378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78623027-C-T

73824398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78623047-A-G

73824398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78623047-A-T

73824650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78623287-G-T

http://identifiers.org/hco/6/GRCh38#73824666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78623303-C-A

http://identifiers.org/hco/6/GRCh38#73824798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78623423-C-A

73824798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78623423-C-T

73824824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78623449-T-C

73825460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78625170-G-A

73825470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78625180-T-C

73825496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78625204-T-C

http://identifiers.org/hco/6/GRCh38#73826132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78626445-C-A

73826141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626454-T-A

73826163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626476-C-G

73826200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626506-A-G

73826206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626512-G-C

73826346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626644-T-C

73826347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626645-G-T

73826417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626709-C-T

73826447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78626739-C-T

73826694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627325-A-G

73826729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627359-G-C

73826754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627384-G-C

73826754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627384-G-T

73826770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627400-A-G

73826776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627406-T-C

73826785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627415-C-T

73826804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627434-G-A

73826804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627434-G-T

73826825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627449-G-C

73826839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627463-G-T

73826841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627465-G-T

73826852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627476-A-T

73826930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627558-C-G

73826966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627594-C-G

http://identifiers.org/hco/6/GRCh38#73827068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78627694-C-A

http://identifiers.org/hco/6/GRCh38#73827099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#78627718-C-A

73827125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627749-A-G

73827137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627760-A-G

73827137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627760-A-T

73827191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627805-C-G

73827306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627915-G-A

73827306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21685
most severe consequence: 3 prime UTR variant
orthologous variants: 78627915-G-T