http://identifiers.org/hco/3/GRCh38#6632202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110356303-C-A

6632246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110356344-G-A

6632246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110356344-G-C

6632344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110356439-G-A

6632344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110356439-G-C

6632466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110356562-T-C

6632583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110356681-C-T

6632986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110357102-C-T

http://identifiers.org/hco/3/GRCh38#6633025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110357152-C-A

6633025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110357152-C-T

6633530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110357698-A-G

6633650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110357982-G-C

6633845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110358166-G-C

http://identifiers.org/hco/3/GRCh38#6633873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110358195-C-A

6633873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110358195-C-G

6634051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110358750-A-G

6634116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110358813-A-G

6634314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359009-A-G

6634408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359113-G-T

6634490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359190-G-T

6634545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359245-G-A

6634575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359280-T-C

6635013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359851-A-T

http://identifiers.org/hco/3/GRCh38#6635015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110359853-A-C

6635016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359854-G-A

6635016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359854-G-C

6635016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359854-G-T

6635051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359889-T-A

6635051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359889-T-C

6635051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359889-T-G

6635052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110359890-A-G

http://identifiers.org/hco/3/GRCh38#6635084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110359922-C-A

6635085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 110359923-A-G

6635156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110359988-C-T

6636600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110360905-A-G

6636639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110360934-G-A

6636675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110360967-A-G

6636909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110361297-A-G

6641666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110368724-G-A

6641762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110368834-T-A

6642028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369059-A-G

6642123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369155-C-G

6642173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369201-G-C

6642401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369432-G-A

6642401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369432-G-T

6642448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369451-C-G

6642592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110369600-A-T

6647363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110377071-A-G

6647371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110377079-C-T

6647502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110377222-A-T

6647753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110377465-C-G

6648288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379114-A-G

6648321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379145-A-G

6648322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379146-A-G

6648347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379173-A-G

6648727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379500-G-A

6648767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379550-C-T

6648847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379630-G-A

6649014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110379800-G-C

http://identifiers.org/hco/3/GRCh38#6649155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110380402-A-C

6657484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110384005-G-A

6657544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110384066-A-G

6657860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110384365-T-A

6657886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110384390-G-A

http://identifiers.org/hco/3/GRCh38#6658090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110386003-C-A

6658090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386003-C-G

http://identifiers.org/hco/3/GRCh38#6658148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110386061-C-A

6658325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386246-A-T

6658328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386249-C-T

6658381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386300-A-T

6658400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386318-G-A

6658530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386442-G-C

6658564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386475-A-G

6658745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386631-C-T

6658765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386652-C-G

http://identifiers.org/hco/3/GRCh38#6658788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110386673-C-A

6658834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386719-T-A

http://identifiers.org/hco/3/GRCh38#6658986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110386903-C-A

6659005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110386927-T-G

http://identifiers.org/hco/3/GRCh38#6659842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110390149-A-C

6659968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110390273-C-G

6659972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110390277-T-A

6660017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110390323-C-T

6669156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391145-A-G

6669171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391160-G-A

6669171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391160-G-T

6669188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391177-C-G

6669220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391209-C-T

6669267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391257-T-C

http://identifiers.org/hco/3/GRCh38#6669273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110391263-A-C

6669354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391333-C-T

6669453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391432-C-G

6669467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391446-G-A

6669467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391446-G-T

6669629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391606-A-G

6669637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391617-G-T

6669647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391627-C-G

6669647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110391627-C-T

6669724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392215-C-G

6669724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392215-C-T

6670084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392567-C-G

6670084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392567-C-T

6670140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392619-A-G

6670234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392702-T-C

6670241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392709-G-A

6670274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392741-G-A

6670306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392776-T-A

http://identifiers.org/hco/3/GRCh38#6670346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110392818-C-A

6670346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392818-C-T

6670622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110392957-A-G

6670723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393048-G-C

6670758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393084-G-A

6670758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393084-G-T

6671024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393378-G-C

6671055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393415-A-G

6671066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393426-G-A

http://identifiers.org/hco/3/GRCh38#6671069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110393429-A-C

6671189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393597-C-G

6671189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393597-C-T

6671203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393611-G-A

6671246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393665-C-T

6671337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393765-C-G

6671337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393765-C-T

6671352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393783-G-A

6671575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110393980-T-C

6671606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110394006-T-C

6671852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110394765-C-G

6671943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110394849-G-T

6672067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110394972-G-A

6672140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395038-T-C

6672233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395127-T-C

6672292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395186-T-A

6672297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395191-A-G

6672336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395228-C-T

6672408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395294-A-G

6672424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395310-A-G

6672427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395313-A-G

6672427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395313-A-T

6672461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395344-T-C

6672470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395353-T-C

6672629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395485-G-A

6672665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395519-T-A

6672665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395519-T-C

6672783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110395632-C-G

6674456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110402599-G-A

6674504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110402648-T-C

6674558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110402702-G-A

6674757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110402862-A-G

6674860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110402943-T-C

6675049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403047-T-A

6675280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403150-C-T

http://identifiers.org/hco/3/GRCh38#6675308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110403178-A-C

6675404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403264-A-G

http://identifiers.org/hco/3/GRCh38#6675435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110403292-C-A

6675640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403458-A-G

6675674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403492-G-C

6675674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403492-G-T

6676019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403814-C-T

6676023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403818-T-C

6676118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403910-C-G

http://identifiers.org/hco/3/GRCh38#6676184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110403978-A-C

6676196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110403990-A-T

6676257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110404048-G-A

6676334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110404130-T-C

http://identifiers.org/hco/3/GRCh38#6678271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110404552-A-C

6678306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110404585-G-A

6678328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110404607-G-A

6678355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110404635-A-G

6678542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110404828-T-G

6678741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405036-A-T

6678752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405047-T-C

6678817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405250-T-G

6678838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405269-A-G

6678956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405379-G-T

6678988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405411-T-C

6679053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110405466-A-G

6679435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110411812-G-C

6679597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110411979-G-A

6679607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110411989-G-T

6679616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412006-C-T

6679648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412035-G-A

6679918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412251-G-A

6679987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412317-G-C

6679999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412329-C-T

6680116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412447-G-T

6680213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412528-T-C

6680260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412575-G-A

6680349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412663-T-A

6680418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412732-G-A

6680597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110412911-G-A

6680768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413066-C-T

6681291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413241-T-G

6681364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413323-T-G

6681574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413563-A-G

6681748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413731-G-A

6681784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413765-A-G

http://identifiers.org/hco/3/GRCh38#6681792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110413773-C-A

6681792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413773-C-T

6681824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413805-C-T

6681897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413870-C-T

6681919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110413892-G-C

6682069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414207-C-G

6682069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414207-C-T

6682088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414227-G-A

6682185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414318-T-C

6682244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414375-T-A

6682389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414486-G-A

6682445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414541-G-A

6682491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414587-G-A

6682518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414614-G-T

6682529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110414625-G-A

6685690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110416593-G-T

http://identifiers.org/hco/3/GRCh38#6685749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110416652-A-C

http://identifiers.org/hco/3/GRCh38#6685857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110416754-C-A

6686075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110416974-G-T

6687133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110419550-A-T

6687306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110419713-A-T

6687329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110419737-C-T

6687346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110419748-G-A

6687378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110419768-A-G

6696182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426129-T-A

http://identifiers.org/hco/3/GRCh38#6696208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110426155-A-C

6696327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426277-A-G

6696350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426297-G-A

6696471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426425-C-T

6696498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426452-G-A

6696498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426452-G-C

6696553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426505-T-C

6696605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426536-T-A

6696663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426595-G-C

6696677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426609-A-T

6696875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426805-G-A

6696957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426887-G-A

6697032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110426963-C-G

6697152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427044-A-T

6697175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427066-G-A

6697474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427374-A-G

http://identifiers.org/hco/3/GRCh38#6697541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427446-C-A

http://identifiers.org/hco/3/GRCh38#6697604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427502-C-A

6697642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427540-T-C

http://identifiers.org/hco/3/GRCh38#6697730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427636-C-A

6697730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427636-C-T

6697733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427639-T-C

6697733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427639-T-G

6697734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427640-T-C

http://identifiers.org/hco/3/GRCh38#6697793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427700-C-A

6697793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427700-C-G

6697793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427700-C-T

6697798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427705-A-G

http://identifiers.org/hco/3/GRCh38#6697864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427747-C-A

6697874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427757-A-T

http://identifiers.org/hco/3/GRCh38#6697929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427798-C-A

6697929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427798-C-T

6697936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427810-G-T

6697940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427814-G-T

6697947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110427821-C-T

http://identifiers.org/hco/3/GRCh38#6697957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110427828-C-A

6698070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427932-C-G

6698089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110427951-A-T

6698228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110429825-T-C

6698281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110429878-A-T

6698285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110429882-T-C

6698354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110429934-A-G

6698378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110429958-G-C

6698378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110429958-G-T

6698455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110430034-T-C

6698568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110430147-C-T

6698721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110430283-C-G

6698721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110430283-C-T

6698888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110430442-G-C

6705851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110431261-T-C

6705924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110431542-A-G

6706245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431837-G-T

http://identifiers.org/hco/3/GRCh38#6706307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110431901-C-A

6706307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431901-C-T

6706309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431903-T-C

6706354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431948-C-T

6706382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431979-G-A

6706382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110431979-G-C

6706533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110432499-C-G

6706562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110432528-A-G

6706703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110432847-T-A

http://identifiers.org/hco/3/GRCh38#6706717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110432861-A-C

6706884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110432983-T-C

6706909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110433018-G-A

6707188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110433219-G-A

6707227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110433258-T-C

6707256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110433287-C-T

6707316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110433350-C-T

6710384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436519-T-A

6710384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436519-T-C

6710407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110436540-A-G

6710418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110436551-T-C

http://identifiers.org/hco/3/GRCh38#6710436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110436569-A-C

6710444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110436577-T-C

6710530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110436662-T-A

6710600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436732-T-A

6710600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436732-T-C

6710670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436802-G-T

6710671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436803-T-C

6710731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436863-G-C

6710801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110436933-G-A

http://identifiers.org/hco/3/GRCh38#6710825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110436955-A-C

6710940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437058-T-C

6710967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437071-C-T

6711029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437133-T-C

6711069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437167-A-G

6711069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437167-A-T

6711082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437180-A-G

http://identifiers.org/hco/3/GRCh38#6711114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110437216-A-C

6711284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437357-C-T

6711321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437392-A-G

6711374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437427-G-A

6711374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437427-G-T

6711499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437551-T-C

6711515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437567-T-C

http://identifiers.org/hco/3/GRCh38#6711555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110437607-C-A

6711662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437699-C-T

6711783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437816-A-T

6711832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437866-A-G

6711844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437879-G-A

6711844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437879-G-C

6711849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437884-C-T

6711897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437929-T-C

6711904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110437936-A-G

6711971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438001-T-A

6711975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438005-A-G

6712008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438047-G-A

6712079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438116-C-T

6712117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438152-C-T

6712166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438185-C-T

6712167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438186-G-A

6712214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438247-C-G

http://identifiers.org/hco/3/GRCh38#6712248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110438304-C-A

6712250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438307-T-A

6712271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438330-A-G

6712335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438443-C-G

6712335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438443-C-T

6712769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110438945-A-G

6712980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110439140-C-T

6713237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110439504-T-A

6713237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110439504-T-C

6713433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110439692-T-C

6713578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110439904-G-A

6713769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110440120-C-T

6714064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110440425-T-A

http://identifiers.org/hco/3/GRCh38#6714101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110440462-C-A

6714101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110440462-C-T

6714195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110440554-G-C

6714302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110440871-A-T

6714688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110441884-A-T

6714916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110442100-G-A

6715120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110442246-C-G

6715210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110442326-A-G

6715271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110442375-G-A

6715273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110442377-A-G

6715331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110442425-C-G

6717101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110444720-C-T

http://identifiers.org/hco/3/GRCh38#6717441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110445054-C-A

6717441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445054-C-T

6717445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445058-G-A

6717445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445058-G-C

6717633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110445279-G-A

6717633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110445279-G-C

http://identifiers.org/hco/3/GRCh38#6717654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110445300-C-A

6717654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110445300-C-T

6717656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110445302-G-T

6717711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445355-T-C

6717846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445503-G-A

6718005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110445660-T-A

http://identifiers.org/hco/3/GRCh38#6718066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110445718-C-A

6723528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110449937-G-T

6723620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450032-A-G

http://identifiers.org/hco/3/GRCh38#6723805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110450222-C-A

6723805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450222-C-T

6723830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450256-T-C

6723830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450256-T-G

6723849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450278-A-G

6723870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450297-G-A

6724038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110450730-A-T

6724292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451058-A-G

6724295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451061-A-G

6724330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451091-T-C

6724368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451133-A-G

http://identifiers.org/hco/3/GRCh38#6724375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110451140-C-A

6724396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451162-T-C

http://identifiers.org/hco/3/GRCh38#6724422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110451183-C-A

http://identifiers.org/hco/3/GRCh38#6724430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110451191-C-A

6724435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451196-C-T

http://identifiers.org/hco/3/GRCh38#6724492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110451251-C-A

6724492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110451251-C-T

6724493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110451252-A-G

6724493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110451252-A-T

http://identifiers.org/hco/3/GRCh38#6724534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110451278-C-A

6724988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451760-T-C

6725008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451778-T-A

6725042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451812-G-A

6725042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451812-G-T

6725055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451825-T-C

6725057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451827-C-G

6725071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451840-G-T

6725101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451870-C-G

6725196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110451969-A-G

http://identifiers.org/hco/3/GRCh38#6725305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110452077-C-A

6725306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452078-A-G

6725306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452078-A-T

6725330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452103-A-G

6725344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452117-G-A

6725377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452149-G-A

6725527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452330-C-T

6725556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452360-G-A

6725557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452361-T-A

6725667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452472-A-G

6725715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452520-A-G

6725858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452670-T-G

6725868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452686-C-T

http://identifiers.org/hco/3/GRCh38#6725874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110452692-A-C

6725952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452757-T-A

6725988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452793-T-C

6725996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452817-T-G

6726142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110452944-T-A

http://identifiers.org/hco/3/GRCh38#6726225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110453011-C-A

6726225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453011-C-G

6726225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453011-C-T

6726323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453097-A-G

6726350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453118-G-T

6726363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453132-C-T

6726370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453139-A-T

6726403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453167-T-C

6726435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453197-T-C

http://identifiers.org/hco/3/GRCh38#6726477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110453240-A-C

6726634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453401-T-C

6726689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110453456-T-A

http://identifiers.org/hco/3/GRCh38#6730796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110454151-C-A

6730857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110454211-A-G

6730887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110454241-A-G

http://identifiers.org/hco/3/GRCh38#6731195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110454551-A-C

6731205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454561-G-T

6731214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454574-A-G

6731214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454574-A-T

6731255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454614-T-G

6731303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454650-G-T

6731335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454682-C-G

6731335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454682-C-T

6731361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110454707-G-T

6731391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110454737-A-G

6731564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110454869-G-C

6731588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110454894-G-C

6731600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110454906-A-G

http://identifiers.org/hco/3/GRCh38#6731813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110455842-A-C

6731821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110455850-T-C

http://identifiers.org/hco/3/GRCh38#6731883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110455884-A-C

6732186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110457308-T-G

6732268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110457372-T-C

6732296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457401-G-C

6732296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110457401-G-T

http://identifiers.org/hco/3/GRCh38#6732424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110457507-C-A

6732552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110457629-C-G

6732552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110457629-C-T

6732626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110457699-C-T

6732797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110457906-T-G

6732905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110458027-T-C

6733105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110458211-C-T

6734469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462317-A-G

6734617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110462431-G-A

6734798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462591-A-G

6735606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110462981-G-A

6735661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 110463037-G-A

6738933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464006-C-T

6739184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464241-A-G

6739270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464335-A-G

6739270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464335-A-T

6739377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464435-G-C

6739414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464475-G-A

6739414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464475-G-T

http://identifiers.org/hco/3/GRCh38#6739441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110464502-C-A

6739441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464502-C-T

6739531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464570-A-G

6739749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110464808-G-T

6739825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110464882-C-G

http://identifiers.org/hco/3/GRCh38#6739828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110464885-C-A

6739843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110464895-C-T

6739849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110464901-G-A

6739849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110464901-G-T

6739906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110464959-G-A

6739906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110464959-G-T

6739950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465003-C-G

6739950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465003-C-T

6740168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465181-A-T

6740211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465233-A-G

6740274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465299-T-C

6740368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465373-A-G

6740486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465478-G-A

6740486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465478-G-T

6740490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465482-G-T

http://identifiers.org/hco/3/GRCh38#6740545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110465537-C-A

6740585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465580-G-A

6740585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465580-G-T

http://identifiers.org/hco/3/GRCh38#6740609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110465605-C-A

6740609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110465605-C-G

6740667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465647-T-A

http://identifiers.org/hco/3/GRCh38#6740696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110465676-C-A

6740702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110465684-G-T

6741026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466201-G-A

6741161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466327-T-C

6741394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466505-C-T

6741425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466538-T-C

6741447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466560-C-G

6741447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466560-C-T

6741472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466585-G-A

6741494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466603-G-A

6741567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466699-C-G

http://identifiers.org/hco/3/GRCh38#6741714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110466826-C-A

6741714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466826-C-T

6741863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466954-A-T

6741904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110466994-C-T

6742189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110467143-C-T

6742247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110467173-G-T

http://identifiers.org/hco/3/GRCh38#6742381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110467305-C-A

6742381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110467305-C-T

6742395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110467319-G-A

6742413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110467337-G-T

http://identifiers.org/hco/3/GRCh38#6742470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110467392-C-A

6742633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110468508-G-T

6742635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110468510-T-A

6742653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110468528-T-G

http://identifiers.org/hco/3/GRCh38#6742733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110468602-C-A

6742912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468781-A-G

6742913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468782-G-A

6742997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468862-G-T

6743021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468886-A-T

6743075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468940-G-A

6743075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468940-G-T

6743084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110468949-T-A

6743238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469077-A-G

6743351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469161-C-G

6743437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469257-C-G

6743527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469483-T-A

6743554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469546-T-C

6743555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469547-T-C

6743660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469633-G-A

http://identifiers.org/hco/3/GRCh38#6743689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#110469650-C-A

6743689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469650-C-T

6743733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469696-A-G

6743835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110469985-T-C

6744359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470476-A-G

6744489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470607-T-A

6744498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470616-G-C

6744560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470674-T-C

6744576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470690-G-C

6744656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470767-C-T

6744767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110470874-A-G

6760282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110493781-G-A

6760361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110493865-T-G

6760403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110493897-C-T

6760577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110494079-A-G

6762500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110494929-A-G

6762718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495138-G-C

6762815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495234-A-G

6762955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495375-C-G

6763018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495450-G-A

6763039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495471-C-T

6763072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495508-A-G

6763095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110495529-A-G

http://identifiers.org/hco/3/GRCh38#6770160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110498128-C-A

6770166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498134-A-G

6770182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498150-T-A

6770182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498150-T-C

6770192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498158-A-G

6770192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498158-A-T

6770236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498179-A-G

6770361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498299-G-A

6770361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498299-G-C

6770361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498299-G-T

6770420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498366-A-T

6770434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498378-C-G

6770436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498380-A-G

http://identifiers.org/hco/3/GRCh38#6770455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110498399-C-A

6770455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498399-C-G

6770464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498408-G-A

6770464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498408-G-C

6770537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498476-T-C

6770988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110498822-T-G

6771249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499074-A-G

6771344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499154-A-G

6771381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499191-C-T

6771433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499240-A-G

6771450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499257-A-G

6771546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499349-A-G

6771633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499434-T-G

6771636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499437-G-A

6771850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499625-G-T

6771955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499728-G-A

6771976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499750-A-G

6771994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499771-T-C

6772015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499791-C-T

http://identifiers.org/hco/3/GRCh38#6772033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110499808-A-C

6772050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110499825-G-A

6776432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110500266-G-A

6776536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110500364-T-C

6776881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110500711-G-A

6776897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110500727-A-G

6776924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110500754-G-A

http://identifiers.org/hco/3/GRCh38#6777019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110500830-A-C

6777312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110503953-C-T

6777497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110504113-T-C

6777563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110504182-A-G

6777766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110506568-G-C

6777896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110506705-T-G

6778299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110507106-A-G

6780011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110509876-A-T

6780138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510007-C-T

http://identifiers.org/hco/3/GRCh38#6780158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110510027-C-A

6780158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510027-C-G

6780158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510027-C-T

6780247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510111-C-T

6780329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510191-A-G

6780347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510209-G-C

6780730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510562-C-T

6780754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510584-C-T

6780851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110510680-C-T

6781974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110511714-G-A

6782177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110511968-A-G

http://identifiers.org/hco/3/GRCh38#6782322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110512104-A-C

6782322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512104-A-T

6782347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512132-T-C

6782347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512132-T-G

6782371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512154-T-C

http://identifiers.org/hco/3/GRCh38#6782400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110512218-A-C

http://identifiers.org/hco/3/GRCh38#6782424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110512244-C-A

6782656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512456-T-C

6782741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512546-T-C

6782861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512658-G-T

6783011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512821-T-G

http://identifiers.org/hco/3/GRCh38#6783014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110512824-A-C

6783093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512902-C-T

6783158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110512965-G-A

6783963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110513181-A-T

6784271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110513485-A-G

6784396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110513628-A-G

6784416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110513648-T-C

6785204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110515354-C-T

6785234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110515380-T-C

http://identifiers.org/hco/3/GRCh38#6785386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110515536-C-A

6785406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110515555-A-G

6785627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110515765-A-G

6786475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516833-G-A

http://identifiers.org/hco/3/GRCh38#6786480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110516838-C-A

6786480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516838-C-T

6786537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516886-G-A

6786563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516907-G-A

6786563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516907-G-T

6786586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 110516930-T-C

6786586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 110516930-T-G

6786607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516939-A-G

http://identifiers.org/hco/3/GRCh38#6786657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110516989-C-A

6786657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110516989-C-T

http://identifiers.org/hco/3/GRCh38#6786690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110517020-C-A

http://identifiers.org/hco/3/GRCh38#6786701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110517042-C-A

6786701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517042-C-T

http://identifiers.org/hco/3/GRCh38#6786727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110517081-C-A

6786727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517081-C-G

6786727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517081-C-T

6786766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517146-G-A

6786784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517164-A-G

6786800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517179-A-G

6786800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517179-A-T

6786945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517332-C-T

6786954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517341-C-G

6787040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517424-A-G

6787074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517467-G-T

6787105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517488-G-T

http://identifiers.org/hco/3/GRCh38#6787196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110517600-A-C

6787196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517600-A-G

6787313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517718-C-G

6787504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110517830-C-G

http://identifiers.org/hco/3/GRCh38#6787601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110517964-A-C

6787638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110518000-A-G

6787667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110518028-C-G

6787997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519222-G-A

6788061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519285-C-G

6788173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519410-A-G

6788190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519426-C-T

6788273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519507-C-T

6788295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519523-T-A

6788374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519602-G-A

6788374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519602-G-C

http://identifiers.org/hco/3/GRCh38#6788456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110519809-C-A

6788456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519809-C-T

6788488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519904-A-G

6788539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519956-T-C

6788539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110519956-T-G

6788803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520235-G-T

6788809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520241-C-T

6788820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520252-T-A

http://identifiers.org/hco/3/GRCh38#6788915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110520345-C-A

6788954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520392-T-A

6789004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520441-G-A

6789017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520454-G-A

6789083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520511-G-A

http://identifiers.org/hco/3/GRCh38#6789322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110520750-C-A

6789554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110520975-G-A

6789651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521070-T-C

6789740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521157-G-T

6789833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521241-G-A

6789887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521296-G-T

6790190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521458-T-G

6790243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521509-A-G

6790297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521588-C-T

6790418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521713-C-T

6790512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521812-A-G

6790621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110521939-G-T

6790760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522075-A-T

6790895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522197-T-G

http://identifiers.org/hco/3/GRCh38#6790969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110522268-C-A

6790969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522268-C-T

6790978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522277-T-C

6790997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522291-A-G

6791021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522315-G-T

6791037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522331-A-G

http://identifiers.org/hco/3/GRCh38#6791040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110522334-C-A

6791078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110522367-T-G

6791097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110522386-A-G

6791460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522766-G-A

6791570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522853-G-T

6791648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522943-C-G

6791648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522943-C-T

6791652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110522947-G-A

http://identifiers.org/hco/3/GRCh38#6794382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110528522-C-A

6794484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110528423-G-A

6794585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110528328-A-G

6794789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110528108-A-G

6794904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110528023-G-A

http://identifiers.org/hco/3/GRCh38#6795306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110527708-C-A

6795333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527689-T-G

6795342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527680-A-G

6795364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527658-A-G

6795498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527531-G-A

http://identifiers.org/hco/3/GRCh38#6795553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110527468-C-A

6795553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527468-C-T

6795648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527374-G-C

6795878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527136-G-T

6795880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527134-G-T

6795883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110527131-G-T

6796049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530182-A-G

6796372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530506-T-C

6796456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530580-C-T

6796532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530650-T-G

http://identifiers.org/hco/3/GRCh38#6796567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110530694-A-C

6796831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530932-A-G

6796831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530932-A-T

6796865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530947-G-A

6796904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110530991-T-C

6796959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110531042-A-G

6796960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110531050-C-G

6797998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110531859-A-G

6798035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110531896-C-G

6798050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110531916-G-A

6798050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110531916-G-T

6798305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110532128-T-C

6799760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110533350-G-C

6799805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110533398-C-G

6799805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110533398-C-T

http://identifiers.org/hco/3/GRCh38#6799836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110533429-C-A

6799935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110533505-A-G

6800056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110533592-A-G

http://identifiers.org/hco/3/GRCh38#6800738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110534332-A-C

6800882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110534460-G-A

6800908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110534486-G-C

6800981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110534554-C-G

6801250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110534834-A-T

6801266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110534839-T-G

6801343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110534916-C-T

6801670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536115-A-G

6801870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536294-G-A

6801902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536316-G-A

http://identifiers.org/hco/3/GRCh38#6802460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110536574-A-C

6802460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536574-A-G

6802570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536687-C-T

http://identifiers.org/hco/3/GRCh38#6802732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110536856-C-A

6802734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536858-A-G

6802848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110536972-T-G

6802922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537028-A-G

http://identifiers.org/hco/3/GRCh38#6803092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110537140-C-A

6803092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537140-C-G

6803092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537140-C-T

6803096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537144-C-T

6803579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537427-G-A

6804084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537946-C-T

6804089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537951-T-A

6804092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110537954-G-A

6804283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110538140-G-C

http://identifiers.org/hco/3/GRCh38#6805247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#110540665-C-A

6805366-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110540748-T-A

6805366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110540748-T-G

6805442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42444
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110540825-G-A