109734188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114723530-A-G

109734306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114723636-G-T

109734322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114723652-G-A

109734322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114723652-G-T

109734379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114723713-G-A

109734379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114723713-G-T

http://identifiers.org/hco/12/GRCh38#109734768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114724091-C-A

109734768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114724091-C-T

109734803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114724135-G-C

109734803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114724135-G-T

109734806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114724139-G-A

109734806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114724139-G-T

109734968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724244-G-A

109734968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724244-G-T

109734977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724253-G-A

http://identifiers.org/hco/12/GRCh38#109734990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114724269-C-A

109734997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724276-G-A

109734997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724276-G-T

109735043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724320-T-C

109735147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724401-C-T

109735161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724405-T-C

109735210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724446-C-T

109735220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724456-G-A

109735272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724504-C-G

109735272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724504-C-T

109735273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724505-G-A

109735273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724505-G-C

109735483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114724689-T-C

109735724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114724875-T-C

109735768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114724907-C-T

109735812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114724944-T-A

109735942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114725104-G-T

109735950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114725112-G-A

109735964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725126-T-C

109735980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725142-A-G

109735998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725155-C-T

109736012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725169-G-A

http://identifiers.org/hco/12/GRCh38#109736020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114725184-C-A

109736020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725184-C-T

109736021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725185-A-G

109736078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725246-T-A

109736079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725247-G-A

109736079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725247-G-T

109736125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114725288-C-G

109736728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114726102-G-A

109736749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114726123-G-T

109736955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726295-A-G

109737055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726378-G-A

http://identifiers.org/hco/12/GRCh38#109737082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114726406-C-A

109737082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726406-C-T

109737083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726407-C-T

109737106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726428-C-G

109737108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726430-G-A

109737269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114726880-C-T

109737433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114727027-T-C

http://identifiers.org/hco/12/GRCh38#109737576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114727128-C-A

109737576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114727128-C-T

109737580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114727132-A-G

109738197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114727614-G-T

109738288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114727656-C-T

109738455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114727826-C-T

109738737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114727968-C-T

109738917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728111-A-G

109738928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728122-C-G

http://identifiers.org/hco/12/GRCh38#109738949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114728143-C-A

109739024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728167-C-G

109739059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728202-G-A

109739069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728212-G-A

109739137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728274-C-T

109739228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728360-C-T

109739491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728579-G-A

109739804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728834-A-G

109739804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114728834-A-T

http://identifiers.org/hco/12/GRCh38#109739892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114728977-A-C

109740093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729190-A-G

109740497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729559-A-T

109740869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729780-T-A

109740885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729791-G-T

109740969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729871-G-A

109740969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729871-G-C

109740979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114729882-G-A

109741114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114730010-G-A

109741223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114730115-C-T

109742374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114730772-A-G

109742414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114730811-G-A

109742558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114730968-C-T

109742745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731185-C-G

109742745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731185-C-T

109742765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731205-C-T

109742830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731269-C-T

109742930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731366-T-C

109742978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731414-C-G

109742998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731432-T-G

109743538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731779-A-T

http://identifiers.org/hco/12/GRCh38#109743580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114731819-C-A

109743580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731819-C-T

109743588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114731827-G-T

109743991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114732209-T-C

http://identifiers.org/hco/12/GRCh38#109744241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114732540-C-A

109745078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114732914-C-T

109745246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733045-A-G

109745277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733076-T-C

109745277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733076-T-G

109745588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733334-C-T

109745691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733395-A-T

109745896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733583-T-C

109745900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733587-C-T

109745903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733590-G-T

109745931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733619-T-G

109745958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733650-A-T

109745975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114733667-G-A

109752856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114739624-C-T

http://identifiers.org/hco/12/GRCh38#109752997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114739790-C-A

109753029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114739820-T-C

109753147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114739947-G-A

109753211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114739980-G-A

http://identifiers.org/hco/12/GRCh38#109757989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114742628-A-C

109758012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114742649-G-T

109758748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114743165-A-T

109758968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114743326-C-T

http://identifiers.org/hco/12/GRCh38#109759161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114743472-A-C

109759454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114743839-T-C

109759543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114743924-C-G

109759543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114743924-C-T

109759640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114744017-C-G

109759721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114744097-C-T

109760837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114744229-G-C

http://identifiers.org/hco/12/GRCh38#109760883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114744283-C-A

109760883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114744283-C-T

109760977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114744313-G-A

109761051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114744372-C-G

109761204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114744518-C-G

http://identifiers.org/hco/12/GRCh38#109762516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114745755-A-C

109762631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114745861-A-G

109764636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114747034-T-C

109764884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114747285-A-G

109765956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114747927-T-C

109766133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748066-G-A

109766226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748174-C-T

http://identifiers.org/hco/12/GRCh38#109766252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114748241-C-A

109767905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748788-G-A

109767905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748788-G-T

109767929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748808-G-A

109767929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748808-G-T

http://identifiers.org/hco/12/GRCh38#109767942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114748819-C-A

109767942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748819-C-T

109767962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748839-A-G

109767980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748858-G-C

109767980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114748858-G-T

109768304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749177-G-T

109768340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749213-A-G

109768343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749216-G-A

109768343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749216-G-T

http://identifiers.org/hco/12/GRCh38#109768550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114749423-C-A

109768550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749423-C-T

http://identifiers.org/hco/12/GRCh38#109768559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114749432-C-A

109768559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749432-C-G

109768559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749432-C-T

109768568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749441-G-A

109768568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749441-G-C

109768568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749441-G-T

109768712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749585-G-A

109768712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749585-G-T

109768761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749634-T-C

109768761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749634-T-G

http://identifiers.org/hco/12/GRCh38#109768811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114749684-A-C

109768811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749684-A-G

109768817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749690-G-A

109768817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749690-G-C

109768817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749690-G-T

109768841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749714-T-A

109768841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749714-T-C

109768841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749714-T-G

109768858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749731-G-A

109768858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749731-G-T

http://identifiers.org/hco/12/GRCh38#109768873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114749752-C-A

109768873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749752-C-T

http://identifiers.org/hco/12/GRCh38#109768904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114749783-C-A

109768904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114749783-C-T

109769258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750137-T-C

109769517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750370-G-A

109769517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750370-G-T

http://identifiers.org/hco/12/GRCh38#109769531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750384-A-C

109769531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750384-A-G

109769531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750384-A-T

109769665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750468-G-A

109769665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750468-G-T

109769820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750568-C-G

109769820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750568-C-T

http://identifiers.org/hco/12/GRCh38#109769832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750591-C-A

109769832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750591-C-T

http://identifiers.org/hco/12/GRCh38#109769841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750599-C-A

http://identifiers.org/hco/12/GRCh38#109769878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750637-A-C

http://identifiers.org/hco/12/GRCh38#109769919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750674-C-A

109769920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750675-T-G

http://identifiers.org/hco/12/GRCh38#109769924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750679-A-C

109769924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750679-A-T

http://identifiers.org/hco/12/GRCh38#109769925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750680-A-C

109769931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750686-G-T

http://identifiers.org/hco/12/GRCh38#109769961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114750715-A-C

109770220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114750997-T-C

109770237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114751013-T-C

http://identifiers.org/hco/12/GRCh38#109770264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#114751036-C-A

109770321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114751103-G-A

109770574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751328-G-A

109770574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751328-G-T

http://identifiers.org/hco/12/GRCh38#109770607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114751355-C-A

109770607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751355-C-G

109770607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751355-C-T

109770608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751356-G-A

http://identifiers.org/hco/12/GRCh38#109770845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#114751567-A-C

109771163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114751854-T-C

109771315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114752041-G-A

109771326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114752052-G-A