195658040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74498369-G-A

195658040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74498369-G-T

195658213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498237-G-A

195658213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498237-G-T

195658220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498230-G-A

195658220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498230-G-C

195658220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498230-G-T

195658236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498212-A-G

195658287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498195-T-C

195658287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498195-T-G

195658296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498186-G-A

195658296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498186-G-T

195658454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498121-C-G

195658454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498121-C-T

195658482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498112-C-G

195658484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74498110-C-T

195658768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497999-G-A

195658768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497999-G-C

195659160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497668-G-A

195659346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74497491-G-T

195659503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74496201-T-G

195660557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493847-C-G

http://identifiers.org/hco/3/GRCh38#195660571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493833-C-A

195660960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493742-C-T

195661010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493695-T-C

195661315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493417-G-T

195661348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493384-G-A

195661553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493213-C-G

195661553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493213-C-T

195661630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493163-G-A

195661630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493163-G-T

195661636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493157-G-T

195661673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493120-G-T

195661676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493117-G-A

195661676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493117-G-T

http://identifiers.org/hco/3/GRCh38#195661697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493100-C-A

195661697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493100-C-G

195661701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493096-G-A

195661701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493096-G-C

195661705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74493092-T-G

http://identifiers.org/hco/3/GRCh38#195661741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74493069-C-A

195661763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74493047-C-T

195661783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74493027-C-T

195661941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492721-A-G

195661943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492719-A-G

195661943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492719-A-T

http://identifiers.org/hco/3/GRCh38#195661949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74492710-C-A

195661949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492710-C-T

195662209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492466-T-C

195662222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492451-C-G

195662222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492451-C-T

195662240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492433-T-C

195662251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492422-C-T

195662314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74492339-T-C

195662367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491797-G-C

http://identifiers.org/hco/3/GRCh38#195662433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74491745-C-A

195662543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491641-G-A

195662543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491641-G-T

http://identifiers.org/hco/3/GRCh38#195662544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74491640-C-A

195662544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491640-C-G

195662544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491640-C-T

http://identifiers.org/hco/3/GRCh38#195662758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74491431-C-A

195662758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491431-C-G

195662758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491431-C-T

195662783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74491412-A-G

195663274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74488129-T-A

195663274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74488129-T-C

195663432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487991-T-C

http://identifiers.org/hco/3/GRCh38#195663503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487939-C-A

195663503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487939-C-T

http://identifiers.org/hco/3/GRCh38#195663573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74487869-C-A

195663573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487869-C-G

195663573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487869-C-T

195663780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487676-A-G

195663780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487676-A-T

195663874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487585-T-C

195663976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487454-G-C

195663976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487454-G-T

195664075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74487339-A-G

195664094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74487320-T-C

195664095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74487319-T-G

195664236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74487178-A-G

195664382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486694-G-T

195664420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486656-G-A

195664515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486569-G-A

195664547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74486536-G-A

195665355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485964-C-G

195665355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485964-C-T

http://identifiers.org/hco/3/GRCh38#195665406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485914-A-C

195665439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485887-G-A

195665481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485855-C-T

195665500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485836-T-C

195665501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485835-T-C

195665559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485775-C-T

195665564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485769-G-A

195665564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485769-G-C

195665564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485769-G-T

195666228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485496-T-A

195666228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485496-T-G

195666237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485487-A-G

195666256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485471-A-G

195666256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485471-A-T

http://identifiers.org/hco/3/GRCh38#195666265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485454-A-C

195666265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485454-A-G

195666265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485454-A-T

195666305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485420-A-G

195666319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485406-G-T

http://identifiers.org/hco/3/GRCh38#195666321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485404-C-A

195666321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485404-C-T

195666326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485399-G-A

195666326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485399-G-T

195666343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485382-T-C

195666344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485381-G-A

195666344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485381-G-T

http://identifiers.org/hco/3/GRCh38#195666477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485282-C-A

195666477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74485282-C-T

http://identifiers.org/hco/3/GRCh38#195666679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74485119-C-A

195666820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484981-A-G

195666925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484895-C-G

195666925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484895-C-T

195667022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74484824-T-C

195668276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482760-A-G

195668305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482734-G-T

195668338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482709-G-A

195668364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482681-G-A

195668364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482681-G-C

195668365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482680-A-G

195668372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482673-T-C

195668372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482673-T-G

195668434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482601-G-A

195668434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482601-G-C

195668434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482601-G-T

195668572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74482484-G-A

195668572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74482484-G-T

195668697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482362-T-A

195668697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482362-T-C

195668705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482354-A-G

195668705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482354-A-T

195670183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482080-C-T

195670226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482041-C-G

195670226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74482041-C-T

195670286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481981-C-T

http://identifiers.org/hco/3/GRCh38#195670352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74481941-C-A

195670352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481941-C-G

195670352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481941-C-T

195670376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481919-G-A

195670376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481919-G-T

195670380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481915-A-G

195670380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481915-A-T

195670412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481884-T-C

195670412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481884-T-G

195670444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481862-T-A

195670462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481845-C-T

195670640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481721-G-A

195670849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481554-G-A

195671108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481338-T-G

195671227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74481212-G-A

195671227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74481212-G-T

195671309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481132-G-A

http://identifiers.org/hco/3/GRCh38#195671316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74481125-C-A

195671316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481125-C-T

195671321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481120-G-A

195671321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481120-G-C

195671321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481120-G-T

http://identifiers.org/hco/3/GRCh38#195671340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74481092-A-C

195671340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481092-A-G

195671340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481092-A-T

195671361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481069-G-T

http://identifiers.org/hco/3/GRCh38#195671413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74481000-C-A

195671413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74481000-C-T

195671437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480977-G-A

195671437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480977-G-T

195671440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480974-T-C

http://identifiers.org/hco/3/GRCh38#195671447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480967-C-A

195671447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480967-C-T

http://identifiers.org/hco/3/GRCh38#195671463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480951-A-C

195671463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480951-A-G

195671463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480951-A-T

195671516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480913-G-A

195671516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480913-G-C

195671516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480913-G-T

http://identifiers.org/hco/3/GRCh38#195671568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480883-C-A

195671568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480883-C-G

195671568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480883-C-T

http://identifiers.org/hco/3/GRCh38#195671697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480755-C-A

195671697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480755-C-G

195672345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480524-G-T

195672381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480487-G-A

195672381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480487-G-T

195672429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480452-A-G

195672429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480452-A-T

195672459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480426-A-G

195672557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74480338-T-A

195672617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74480278-A-G

195672623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74480272-G-A

http://identifiers.org/hco/3/GRCh38#195672738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74480196-C-A

195672738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480196-C-G

195672738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480196-C-T

195672747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480187-G-C

195672747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480187-G-T

195672755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480179-A-G

195672756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480178-G-A

195672756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480178-G-C

195672756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480178-G-T

195672774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480160-A-G

195672799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480144-T-A

195672799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480144-T-C

195672807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480136-G-T

195672826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480130-T-C

195672826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480130-T-G

195672872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480075-T-A

195672899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480029-G-C

195672923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480005-C-G

195672923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74480005-C-T

195673035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479952-G-A

http://identifiers.org/hco/3/GRCh38#195673054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479934-C-A

http://identifiers.org/hco/3/GRCh38#195673113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479880-C-A

195673113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479880-C-G

195673113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479880-C-T

195673192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479828-C-T

195673241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479783-A-G

195673322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479730-G-A

http://identifiers.org/hco/3/GRCh38#195673325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479727-A-C

195673750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479650-G-A

195673750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479650-G-T

http://identifiers.org/hco/3/GRCh38#195673765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479636-C-A

195673765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479636-C-T

http://identifiers.org/hco/3/GRCh38#195673776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479625-A-C

195673776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479625-A-G

195673783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479618-T-A

195673783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479618-T-C

http://identifiers.org/hco/3/GRCh38#195673827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479578-C-A

195673827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74479578-C-T

http://identifiers.org/hco/3/GRCh38#195673848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479557-A-C

http://identifiers.org/hco/3/GRCh38#195673857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479548-A-C

195673857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74479548-A-G

195673857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74479548-A-T

195673884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74479521-T-A

195673884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74479521-T-C

http://identifiers.org/hco/3/GRCh38#195674026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74479375-C-A

195674026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74479375-C-T

195674690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478435-T-G

195674698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478427-A-G

195674777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478361-C-T

195674891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478252-A-G

195674902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478241-C-T

195674910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478233-C-G

195675071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478092-C-T

195675099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74478071-T-A

195675314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74477886-A-G

195675323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74477877-G-A

195675388-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74477844-G-C

195675473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74477767-T-C

195675677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74477566-T-G

195675740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74477498-A-G

195677055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476835-C-G

195677055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476835-C-T

http://identifiers.org/hco/3/GRCh38#195677067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74476823-A-C

195677125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476767-A-G

195677135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476757-C-T

195677590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476666-G-A

195677590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476666-G-T

http://identifiers.org/hco/3/GRCh38#195677638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74476618-C-A

195677638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476618-C-T

195677662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476597-A-G

195677685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74476568-T-C

http://identifiers.org/hco/3/GRCh38#195677739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74476520-C-A

195677739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476520-C-T

195677765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476494-G-A

195677765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476494-G-C

195677765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476494-G-T

195677777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476482-A-G

195677777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476482-A-T

http://identifiers.org/hco/3/GRCh38#195677828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74476434-C-A

195677828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476434-C-G

195677828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74476434-C-T

http://identifiers.org/hco/3/GRCh38#195680983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475653-A-C

195680983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475653-A-G

195680983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475653-A-T

http://identifiers.org/hco/3/GRCh38#195681161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475501-A-C

195681161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475501-A-T

195681181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475482-G-T

195681292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475373-T-A

195681292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475373-T-G

195681319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475346-T-A

195681319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475346-T-C

195681387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475287-G-C

195681387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475287-G-T

195681406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475269-G-A

http://identifiers.org/hco/3/GRCh38#195681572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475138-A-C

195681572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475138-A-G

195681572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475138-A-T

http://identifiers.org/hco/3/GRCh38#195681589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475121-C-A

195681589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475121-C-G

195681589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475121-C-T

195681592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475118-T-A

195681592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475118-T-C

195681592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475118-T-G

195681634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475076-T-A

195681634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475076-T-C

195681634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475076-T-G

195681643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475067-G-A

195681643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475067-G-C

195681643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74475067-G-T

195681668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 74475042-T-G

195681674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74475037-T-C

195681674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74475037-T-G

195681680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475031-C-T

195681683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475028-C-T

http://identifiers.org/hco/3/GRCh38#195681699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74475013-C-A

195681700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475012-C-G

195681700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475012-C-T

195681724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74475001-C-T

195681751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474973-T-A

195681751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474973-T-C

195681751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474973-T-G

195681753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474971-T-G

http://identifiers.org/hco/3/GRCh38#195681774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74474951-A-C

195681774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474951-A-T

195681867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474874-G-A

195681867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74474874-G-T

195682265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473138-T-A

195682265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473138-T-C

195682308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473111-G-C

195682318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473101-T-C

http://identifiers.org/hco/3/GRCh38#195682357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74473088-C-A

http://identifiers.org/hco/3/GRCh38#195682364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74473085-C-A

195682364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473085-C-T

195682472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473002-G-A

195682472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74473002-G-C

195683469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472287-A-T

195683565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472202-A-T

195683609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472173-T-A

195683609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472173-T-C

195683609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472173-T-G

195683626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472154-T-C

195683626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472154-T-G

195683657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472142-G-C

195683657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472142-G-T

195683698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472116-T-C

195683701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74472113-T-C

http://identifiers.org/hco/3/GRCh38#195683806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74472017-C-A

195683806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74472017-C-T

195683833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: non coding transcript exon variant
orthologous variants: 74471990-A-G

http://identifiers.org/hco/3/GRCh38#195683999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74471841-C-A

195683999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471841-C-T

195684043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471801-A-G

http://identifiers.org/hco/3/GRCh38#195684069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74471777-C-A

195684069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471777-C-T

195684072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471773-A-G

195684109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471734-A-G

195684109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471734-A-T

195685774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471336-T-G

195685801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471309-A-G

195685801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471309-A-T

http://identifiers.org/hco/3/GRCh38#195685893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#74471215-C-A

195685893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471215-C-T

195685949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471164-T-A

195685949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471164-T-C

195685949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471164-T-G

195686061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74471040-C-T