200917497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 136139075-T-C

200917505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 136139067-G-T

200917614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 136138949-C-G

200919586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136137167-G-T

http://identifiers.org/hco/1/GRCh38#200919825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136136913-A-C

200919998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136823-C-T

200920609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136506-G-T

200920738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136426-C-T

http://identifiers.org/hco/1/GRCh38#200920794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136136373-C-A

200920878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136350-A-G

200920878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136350-A-T

200920885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136343-G-A

200920885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136343-G-T

200920890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136338-G-C

200920890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136338-G-T

200921128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136137-C-G

200921209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136136092-G-T

http://identifiers.org/hco/1/GRCh38#200921247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136136076-C-A

http://identifiers.org/hco/1/GRCh38#200921311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136136012-C-A

200921311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136136012-C-T

200921366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135958-G-T

200921478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135849-G-A

200921478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135849-G-T

http://identifiers.org/hco/1/GRCh38#200921486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136135841-C-A

200921549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135792-G-T

http://identifiers.org/hco/1/GRCh38#200921696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136135654-C-A

200921701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135649-G-A

http://identifiers.org/hco/1/GRCh38#200921715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136135635-C-A

200921788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136135562-T-C

http://identifiers.org/hco/1/GRCh38#200921796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136135554-C-A

200921921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135424-T-C

200921928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135416-T-A

http://identifiers.org/hco/1/GRCh38#200921957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136135387-C-A

200921957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135387-C-G

200921957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135387-C-T

200922061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135307-T-C

200922153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136135219-G-A

200922632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134783-G-A

200922632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134783-G-T

200922642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134771-G-A

200922770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134644-C-T

200922819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134599-G-T

200922830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134588-A-G

200923044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134445-T-A

200923060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136134429-T-C

200923926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136133637-C-G

200923926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136133637-C-T

200928264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136128831-G-T

200928476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128622-C-T

200928488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128608-G-A

200928488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128608-G-T

200928557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128543-G-A

200928557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128543-G-T

200928706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128412-C-G

200928834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128297-A-G

200928834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128297-A-T

200928897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128245-T-C

200928938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136128205-G-T

200929007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136128136-A-G

200929007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136128136-A-T

200929171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136128003-A-G

200929179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127995-G-A

200929179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127995-G-T

200929192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127982-T-C

http://identifiers.org/hco/1/GRCh38#200929194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136127980-A-C

200929279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127892-G-A

200929335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127845-G-A

200929813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127423-G-T

200929853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127385-A-G

200929860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127378-T-C

200929866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127372-T-C

http://identifiers.org/hco/1/GRCh38#200929994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136127244-C-A

200930000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127239-G-A

200930000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127239-G-C

200930000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127239-G-T

200930025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127206-A-G

200930061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127172-G-A

200930061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127172-G-T

200930097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127156-T-C

http://identifiers.org/hco/1/GRCh38#200930099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136127155-C-A

200930168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136127083-T-C

200931240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136126774-T-C

200931796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136126420-A-G

200931852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136126364-G-T

200932040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136126203-C-G

http://identifiers.org/hco/1/GRCh38#200932128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136126115-A-C

200932217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136126029-G-T

http://identifiers.org/hco/1/GRCh38#200932350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136125902-C-A

200932350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136125902-C-T

200932387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136125865-T-C

200932438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136125814-T-C

200932480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136125789-G-T

http://identifiers.org/hco/1/GRCh38#200932525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136125739-C-A

200932578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136125679-A-G

200932727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136125523-A-G

200937038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136124286-A-G

http://identifiers.org/hco/1/GRCh38#200937066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136124259-C-A

200937066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136124259-C-T

200937134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136124202-T-C

200937225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136124113-A-G

200947777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120276-A-G

200947813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120240-A-G

200948005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120058-G-A

200948005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120058-G-T

200948021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120046-G-A

200948021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120046-G-T

http://identifiers.org/hco/1/GRCh38#200948032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136120035-C-A

200948032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120035-C-T

200948047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136120021-T-C

http://identifiers.org/hco/1/GRCh38#200948064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136120011-C-A

200948144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136119934-A-G

200948196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136119882-A-G

http://identifiers.org/hco/1/GRCh38#200948245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136119830-A-C

200948245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119830-A-G

200948245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119830-A-T

200948284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119804-C-T

200948355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119730-G-A

200948653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119455-G-C

200948680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119436-C-G

200948820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136119297-G-A

200948835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136119285-G-T

http://identifiers.org/hco/1/GRCh38#200948865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136119255-C-A

200948898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136119211-T-C

200949402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118883-G-A

http://identifiers.org/hco/1/GRCh38#200949404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136118882-C-A

200949404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118882-C-T

http://identifiers.org/hco/1/GRCh38#200949408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136118878-C-A

200949484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118816-T-C

http://identifiers.org/hco/1/GRCh38#200949529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136118776-C-A

200949529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118776-C-T

200949538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118767-C-T

200949637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118668-A-G

200949642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118663-G-A

200949642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118663-G-T

200949690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118616-G-A

200949690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118616-G-T

200949721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118586-G-A

200949721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118586-G-T

200949725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118582-A-G

http://identifiers.org/hco/1/GRCh38#200949820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136118488-C-A

200949820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118488-C-T

200949825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136118483-G-T

200949932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136118378-C-T

http://identifiers.org/hco/1/GRCh38#200949943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136118367-C-A

200952437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136116632-T-C

200952454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136116615-G-A

200952497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136116569-C-T

200956332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114833-T-C

200956496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114671-T-C

http://identifiers.org/hco/1/GRCh38#200957269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136114571-C-A

200957269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114571-C-T

200957283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114553-G-T

http://identifiers.org/hco/1/GRCh38#200957357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136114479-C-A

http://identifiers.org/hco/1/GRCh38#200957436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136114400-C-A

200957436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136114400-C-T

200957492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114343-A-G

200957644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114198-T-A

200957644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114198-T-C

200957696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114146-A-G

200957721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114126-G-A

200957721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114126-G-T

200957749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114102-G-T

200957783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114068-G-A

200957783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114068-G-T

200957806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114050-T-C

http://identifiers.org/hco/1/GRCh38#200957812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136114044-C-A

200957812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 136114044-C-T

http://identifiers.org/hco/1/GRCh38#200957852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136114005-C-A

200957852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136114005-C-T

200957896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113961-C-T

http://identifiers.org/hco/1/GRCh38#200957968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136113910-C-A

200957968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113910-C-G

200957968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113910-C-T

http://identifiers.org/hco/1/GRCh38#200957995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136113888-C-A

http://identifiers.org/hco/1/GRCh38#200958056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136113826-C-A

200958056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136113826-C-T

200958204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113678-A-G

200958204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113678-A-T

200958209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113674-T-A

200958209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113674-T-C

200958209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113674-T-G

200958247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113625-T-G

200958949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136113227-G-A

200958980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136113196-T-G

200959066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113116-G-T

200959077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113105-G-A

200959077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136113105-G-T

200959585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136112834-G-A

http://identifiers.org/hco/1/GRCh38#200959887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136112610-C-A

200960154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136112274-C-T

200960180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136112246-T-C

200960314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136112120-A-G

200960314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136112120-A-T

200960326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136112109-T-C

http://identifiers.org/hco/1/GRCh38#200960327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136112108-C-A

200960332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 136112102-A-G

http://identifiers.org/hco/1/GRCh38#200960352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136112082-C-A

200960352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136112082-C-T

200960389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136112045-G-T

http://identifiers.org/hco/1/GRCh38#200960422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136112012-C-A

200960451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111980-T-C

http://identifiers.org/hco/1/GRCh38#200960486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136111959-C-A

200960595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111896-T-G

200964852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111349-T-G

http://identifiers.org/hco/1/GRCh38#200965005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136111186-C-A

200965005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111186-C-T

200965014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111175-G-A

200965014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111175-G-T

200965022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111167-T-C

http://identifiers.org/hco/1/GRCh38#200965094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136111095-C-A

200965094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136111095-C-T

200965115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136111074-G-C

200965156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136111030-A-G

200965196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110990-G-A

200965365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110844-C-T

200965500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110701-G-A

200965609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110594-A-G

200965613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110592-A-G

http://identifiers.org/hco/1/GRCh38#200965659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136110560-C-A

http://identifiers.org/hco/1/GRCh38#200965703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136110520-C-A

200965809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110414-G-A

200965809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110414-G-C

200965813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110410-C-T

200965903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110330-T-C

200965906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110327-T-C

http://identifiers.org/hco/1/GRCh38#200965977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136110256-C-A

200965977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110256-C-T

200966095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136110131-C-T

200966166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136109919-T-C

200966193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136109891-G-A

200966193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136109891-G-T

http://identifiers.org/hco/1/GRCh38#200966326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#136109754-C-A

200966371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136109690-T-C

200966383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 136109678-A-G

200966464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136109597-G-A

200966480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33122
most severe consequence: non coding transcript exon variant
orthologous variants: 136109581-G-A