66413003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78166034-G-T

66413021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78166052-A-G

66413158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78166200-G-A

66413519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78166507-T-C

66413576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78166559-A-G

66413812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78166793-G-C

66414073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167050-T-A

66414188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167175-G-C

66414188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167175-G-T

http://identifiers.org/hco/14/GRCh38#66414205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78167192-A-C

66414221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167208-G-A

66414246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167233-T-C

66414259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167246-T-C

66414313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167299-T-A

66414388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167416-T-C

66414403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167431-G-T

66414828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167833-T-C

66414887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78167892-G-T

66415158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78168160-C-T

66415178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78168176-G-A

66415206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78168201-G-A

66415409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78168597-G-T

66415554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78168719-G-A

66417494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78173152-A-G

66417763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78173413-A-G

66418116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78173673-T-C

66418153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78173688-T-G

66418184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78173699-A-G

66418386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78173822-G-T

66418575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78174159-T-C

66418782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78174358-C-T

66419190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78175051-A-T

66419245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78175105-A-G

66419256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78175116-G-A

66419271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78175123-G-C

66420705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78176917-G-A

66420934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78177163-T-A

http://identifiers.org/hco/14/GRCh38#66421101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78177743-A-C

66421132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78177776-C-T

66421338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78177971-T-C

66421426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178032-G-A

66421434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178040-C-T

66421725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178313-G-A

66421817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178405-C-T

66421868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178462-G-T

66421923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178518-T-C

66422037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178629-T-C

66422055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178647-G-C

66422196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78178785-C-T

66422569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78179164-C-T

66425392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180094-C-G

66425419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180121-A-G

66425419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180121-A-T

66425666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180384-G-A

66425666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180384-G-T

66425668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180386-T-C

66425803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180523-A-G

66426103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180794-T-A

66426241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78180931-T-C

66426423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78181114-G-A

66426616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78181292-G-A

66426760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78181424-G-A

66426966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78181795-T-C

66427019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78181875-G-A

66427031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78181887-G-C

66428212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78182954-A-G

66428357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78183082-T-C

66428677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78183347-G-A

66428748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78183457-G-A

66428761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78183470-T-C

66428882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78183587-C-G

66429247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78184700-T-G

66430107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78185599-T-C

66430362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78185867-G-A

66431030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78186445-G-A

66431600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78186975-C-T

66431795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78187173-A-T

66434994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78190221-A-G

http://identifiers.org/hco/14/GRCh38#66435139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78190363-A-C

66435139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78190363-A-G

66436552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78191652-C-T

66436703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78191786-A-G

66436746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78191827-G-T

66437231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78192046-G-A

66441619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78196138-G-A

66442181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78196653-T-A

66442433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78196898-G-A

66442466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78196930-C-G

66442663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78197114-G-A

66442977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78197402-C-T

66443045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78197470-T-C

http://identifiers.org/hco/14/GRCh38#66443762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78198191-C-A

66443884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198287-C-G

66443888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198291-T-C

66443918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198317-C-T

66444138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198537-G-A

66444180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198568-T-C

66444349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198769-T-A

66444493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78198923-C-G

http://identifiers.org/hco/14/GRCh38#66444527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78198956-A-C

66444573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199002-C-T

66444700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199125-C-T

66444702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199127-G-A

66444832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199257-C-T

66444849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199274-G-T

66444861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199286-C-T

66445010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199438-G-A

66445026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199455-G-A

66445230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199644-T-A

66445325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199739-A-G

66445329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199743-C-G

66445458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78199877-T-C

66445809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78200254-C-G

66445809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78200254-C-T

66446200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78200656-C-G

66446200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78200656-C-T

66446537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78201019-C-T

http://identifiers.org/hco/14/GRCh38#66446556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78201038-C-A

http://identifiers.org/hco/14/GRCh38#66446717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78201456-A-C

66447781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78201740-C-T

66447924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78201883-G-A

66447956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78201915-T-G

66448096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78202051-T-C

66448277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78202236-T-A

66448502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78202464-C-T

http://identifiers.org/hco/14/GRCh38#66448544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78202513-C-A

66448544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78202513-C-G

66448593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78202562-A-G

66448866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78202828-C-T

http://identifiers.org/hco/14/GRCh38#66449078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78203347-A-C

http://identifiers.org/hco/14/GRCh38#66449131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78203439-C-A

66449131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78203439-C-T

http://identifiers.org/hco/14/GRCh38#66449217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78203526-C-A

66450069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78204700-T-C

http://identifiers.org/hco/14/GRCh38#66450120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78204751-C-A

66450494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205129-T-C

66450584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205218-C-T

66450605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205228-C-T

66450628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205252-A-G

http://identifiers.org/hco/14/GRCh38#66450670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78205294-A-C

66450897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205526-T-C

http://identifiers.org/hco/14/GRCh38#66451117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78205748-A-C

66451117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205748-A-T

66451518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205903-G-C

66451540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205929-T-A

66451603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78205991-G-A

66451615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78206003-G-C

66451768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78206171-C-T

66452038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78206331-G-A

66453608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78209196-G-A

66453727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78209321-A-T

http://identifiers.org/hco/14/GRCh38#66453729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78209323-C-A

66454026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78209597-G-A

66454238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78209778-T-C

66455215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78210908-T-C

66458852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78216579-T-C

66458852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78216579-T-G

66458896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78216612-C-T

66459241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78217393-C-T

66460868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78218736-T-A

66460910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78218761-T-C

66461024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78218889-T-C

66461599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78219164-A-G

66461599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78219164-A-T

66461976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78219469-A-G

http://identifiers.org/hco/14/GRCh38#66462174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78219673-C-A

66462393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78219849-C-T

66462485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78219942-T-C

http://identifiers.org/hco/14/GRCh38#66462645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78220105-C-A

66463398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78220557-C-T

66463960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78220806-G-A

66463976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78220822-T-C

66464697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78221508-T-C

http://identifiers.org/hco/14/GRCh38#66465440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78222148-C-A

66472099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78222278-A-T

http://identifiers.org/hco/14/GRCh38#66472122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78222296-C-A

66472906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78223092-T-G

http://identifiers.org/hco/14/GRCh38#66473080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78223261-C-A

66473239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78223441-T-C

66473266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78223468-T-A

66473286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78223492-G-T

66473652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78223883-A-G

66476113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78229957-G-T

66476201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78230051-T-C

66476661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78230489-T-C

66476762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78230586-T-A

http://identifiers.org/hco/14/GRCh38#66476950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78230868-A-C

66477004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78230918-T-C

http://identifiers.org/hco/14/GRCh38#66477295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78232316-A-C

66477691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78232715-T-C

66477985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78232996-A-G

66478051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233297-G-C

66478158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233404-A-G

66478236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233481-T-C

66478394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233634-G-A

66478535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233769-T-C

66478566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233799-G-T

66478576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78233809-T-C

66479265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78234850-A-G

66479395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78234997-C-T

http://identifiers.org/hco/14/GRCh38#66479433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78235033-C-A

http://identifiers.org/hco/14/GRCh38#66480892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78235942-C-A

66480942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78235986-A-G

66480951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78235995-A-G

66481049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78236094-A-G

66482654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78239214-C-T

66483067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78239455-T-C

66483263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78239644-C-T

66483904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78240898-C-T

66483917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78240911-T-C

66484355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241136-A-G

66484971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241446-A-G

66485175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241633-G-A

66485176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241634-T-C

66485247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241693-G-A

66485343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241779-C-T

66485380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241818-C-G

66485503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78241942-A-G

66486243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78243690-T-C

66486315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78243762-G-A

66486315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78243762-G-T

66486574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78244016-C-T

66486724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78244163-C-T

66486836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78244274-G-A

66486836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78244274-G-C

66486859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78244297-G-T

http://identifiers.org/hco/14/GRCh38#66486866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78244304-A-C

66486876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78244314-C-T

66487357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78244765-T-C

http://identifiers.org/hco/14/GRCh38#66487507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78244879-A-C

66487527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78244893-G-A

66488046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78245309-G-A

66488046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78245309-G-T

66488095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78245358-T-C

66488141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78245403-A-G

66488230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 78245493-G-T

66489009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78246509-G-A

66489009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78246509-G-C

66489009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78246509-G-T

http://identifiers.org/hco/14/GRCh38#66489083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78246578-A-C

66489129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78246625-T-C

66489134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78246629-T-C

http://identifiers.org/hco/14/GRCh38#66489259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78246740-C-A

66489259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78246740-C-T

66489299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247004-C-T

66489315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247020-T-G

66490617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247637-A-G

http://identifiers.org/hco/14/GRCh38#66490718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78247717-C-A

66490730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247729-G-A

66490730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247729-G-T

http://identifiers.org/hco/14/GRCh38#66490763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78247762-A-C

http://identifiers.org/hco/14/GRCh38#66490795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78247794-C-A

66490903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247893-T-C

66490937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78247912-G-T

http://identifiers.org/hco/14/GRCh38#66490975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78247950-C-A

http://identifiers.org/hco/14/GRCh38#66490979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78247954-C-A

66491015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78247990-T-G

66491069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78248044-A-G

66491092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78248067-G-T

66491095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78248070-G-A

66491148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248122-A-G

66491195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248154-C-T

66491197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248156-C-T

66491198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248157-T-C

66491263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248206-T-C

66491272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248215-T-A

66491324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248272-C-T

http://identifiers.org/hco/14/GRCh38#66491543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78248478-C-A

66491615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78248550-T-C

66491651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 78248586-G-A

66491677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78248612-A-T

66491933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248901-C-G

66491951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78248919-G-T

66492052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 78249012-G-T

66492094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78249054-C-T

66492275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78249235-C-T

66492671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78249329-T-A

http://identifiers.org/hco/14/GRCh38#66492769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78249427-C-A

66492794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78249452-C-T

66492832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78249486-T-C

http://identifiers.org/hco/14/GRCh38#66492853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78249505-C-A

http://identifiers.org/hco/14/GRCh38#66492858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78249510-C-A

http://identifiers.org/hco/14/GRCh38#66492864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78249516-C-A

66492900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78249552-G-T

http://identifiers.org/hco/14/GRCh38#66492950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78249601-C-A

66493088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78249730-G-T

66493180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78249824-G-A

66493639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250256-T-G

66493671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250281-G-A

66493671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250281-G-T

66494052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250640-T-G

66494156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250737-G-A

66494292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250849-C-G

66494292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78250849-C-T

http://identifiers.org/hco/14/GRCh38#66495536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78252639-C-A

66495536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78252639-C-G

66495542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78252645-G-A

66495555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78252658-T-A

66495745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78252857-G-A

66495745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78252857-G-C

66495745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78252857-G-T

66495994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78253123-T-G

http://identifiers.org/hco/14/GRCh38#66496113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78253231-C-A

66496186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78253303-T-C

http://identifiers.org/hco/14/GRCh38#66496387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78253483-C-A

66496387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78253483-C-T

66496593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78253679-G-A

66496637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78253725-G-A

66496826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 78253869-G-C

66497140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78254125-A-G

66497157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78254140-T-G

66497213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78254190-T-C

66497524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78254499-T-C

66497995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255156-G-A

66497995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255156-G-T

http://identifiers.org/hco/14/GRCh38#66497997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78255158-A-C

66498012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255173-C-G

66498012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255173-C-T

http://identifiers.org/hco/14/GRCh38#66498022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78255188-C-A

66498022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255188-C-T

http://identifiers.org/hco/14/GRCh38#66498083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#78255230-C-A

66498083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255230-C-T

66498278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255430-T-C

66498289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255456-C-T

66498290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255457-A-G

66498290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255457-A-T

66498306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78255479-T-C

66498370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78255614-G-C

66498451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20100
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78255699-A-T