http://identifiers.org/hco/8/GRCh38#90791777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15149024-C-A

90791777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15149024-C-G

90791777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15149024-C-T

90791865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15148936-G-T

90791866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 15148935-A-T

90791908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15148893-T-C

90791929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15148872-T-A

http://identifiers.org/hco/8/GRCh38#90791945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15148856-C-A

90791945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15148856-C-T

http://identifiers.org/hco/8/GRCh38#90791948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15148853-C-A

90792061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15148745-A-G

90792061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15148745-A-T

90792120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15148659-G-A

90792120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15148659-G-T

http://identifiers.org/hco/8/GRCh38#90792188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15148595-C-A

90792190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148593-C-G

90792218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148566-C-G

90792231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148553-T-G

90792433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148406-C-T

90792440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148399-C-T

90792494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148345-G-A

90792494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148345-G-T

90792626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148207-G-T

90792712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148132-T-C

90792733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148113-C-T

90792762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148087-C-T

90792786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148063-A-G

90792806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148039-C-T

90792833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148011-C-T

90792835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15148009-T-C

90792902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147940-C-T

90792969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147866-T-C

90793019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147816-G-A

90793019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147816-G-C

90793573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147290-A-G

90793642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147241-G-T

90793703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147182-A-G

90793746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15147139-A-G

90794499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15146327-A-G

90794625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15146187-A-T

90794845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145990-G-T

90794862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145979-T-C

90795033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145805-A-G

90795054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145776-G-A

90795162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145682-G-A

90795186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145658-T-C

90795311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145528-C-G

90795314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145525-T-A

90795317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145522-C-T

http://identifiers.org/hco/8/GRCh38#90795423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15145322-A-C

90795442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145303-G-T

90795443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145302-T-C

90795475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145272-A-G

90795593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145168-G-T

90795735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15145053-C-T

http://identifiers.org/hco/8/GRCh38#90795781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15145007-A-C

90796587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15144537-A-G

90796695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15144437-G-A

90797084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15144060-G-A

90797265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15143891-G-T

http://identifiers.org/hco/8/GRCh38#90797284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15143876-C-A

90797284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15143876-C-T

90797291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15143869-A-G

90797308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15143852-T-A

90797724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15143429-T-C

90797962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15143214-C-T

90801240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140852-C-T

90801310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140781-T-A

90801370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140725-C-T

90801419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140676-T-C

90801606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140493-T-G

90801668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140269-A-G

90801668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140269-A-T

90801768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140170-A-G

90801788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140156-G-A

90801788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140156-G-T

http://identifiers.org/hco/8/GRCh38#90801799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15140145-C-A

90801799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140145-C-G

90801813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140131-T-A

90801813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140131-T-G

90801932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15140011-G-C

90801993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139960-T-A

90802239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139794-G-A

90802296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139741-G-A

90802303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139734-G-A

90802425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139610-C-T

90802639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139442-T-C

90802654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139427-C-T

http://identifiers.org/hco/8/GRCh38#90802841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15139243-C-A

90803202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139234-G-C

http://identifiers.org/hco/8/GRCh38#90803243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15139193-C-A

http://identifiers.org/hco/8/GRCh38#90803422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15139018-A-C

90803422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139018-A-T

90803432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139007-C-T

http://identifiers.org/hco/8/GRCh38#90803433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15139006-C-A

90803433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15139006-C-T

90803447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15138992-T-G

90803455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15138984-A-G

90803582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15138821-G-T

90803633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15138759-C-T

90803640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15138752-T-A

90803654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15138738-C-T

90803825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15138567-G-A

90803930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15138483-C-G

90804761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15138215-C-G

90804905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15138094-T-C

90805260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137793-T-G

90805340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137713-G-T

90805420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137641-G-C

90805451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137616-G-T

90805482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137583-A-G

90805578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137484-G-A

90805704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137373-C-T

http://identifiers.org/hco/8/GRCh38#90805803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15137260-A-C

90805866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137200-G-A

90805899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137167-A-G

90805909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137156-G-A

90805987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15137078-G-A

90806203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15136876-C-T

90806215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15136864-G-C

90806215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15136864-G-T

90806244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15136829-T-C

90806349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15136762-G-A

90806578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15136543-A-G

90806586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15136535-T-C

90806623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15136502-G-A

90806623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15136502-G-T

90806706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15136419-T-C

http://identifiers.org/hco/8/GRCh38#90806889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15135236-A-C

90806937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15135189-C-G

90807189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134974-T-C

90807190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134973-A-G

90807206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134957-A-G

90807245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134918-T-C

90807406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134772-G-A

90807444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134748-G-C

90807496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134706-G-A

90807561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134644-G-A

90807631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134576-G-A

90807686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134518-C-T

90807816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134406-C-T

http://identifiers.org/hco/8/GRCh38#90807960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15134291-A-C

90808099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134154-T-C

90808100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134153-A-G

90808166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134087-A-G

90808261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15134000-G-A

90808300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133981-T-C

90808374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133934-G-C

90808381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133927-G-A

90808414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133899-C-T

90809006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133637-A-G

90809014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133629-C-T

90809019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133624-C-T

90809068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133574-C-T

90809116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15133525-G-A

http://identifiers.org/hco/8/GRCh38#90809220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15130426-C-A

http://identifiers.org/hco/8/GRCh38#90809230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15130417-C-A

90809379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15130289-C-G

90809438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15130241-A-G

90809697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15129995-G-C

90810388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15128737-G-A

90810572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15128565-G-A

90812078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15127752-C-G

90812275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15127580-C-G

90812809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15126052-A-G

90812809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15126052-A-T

http://identifiers.org/hco/8/GRCh38#90812864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15125995-C-A

90820459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15124720-T-C

90820490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15124690-A-T

90820906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15123810-C-T

90820951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15123776-C-G

90820979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15123748-T-G

http://identifiers.org/hco/8/GRCh38#90821108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15123622-C-A

90821411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15123142-C-T

http://identifiers.org/hco/8/GRCh38#90821628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15122941-C-A

90821775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15122802-A-G

90822118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15115248-C-T

90822182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15115189-T-G

http://identifiers.org/hco/8/GRCh38#90822291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15115086-C-A

90822291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15115086-C-T

http://identifiers.org/hco/8/GRCh38#90822408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15114978-A-C

90822541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114846-A-G

90822584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114814-G-A

90822713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114696-G-A

90822736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114673-A-T

90822737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114672-C-T

90823010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114359-T-C

http://identifiers.org/hco/8/GRCh38#90823156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15114246-C-A

90823176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114221-T-C

90823189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114206-C-T

90823200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114198-G-A

90823243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114159-C-T

90823295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15114118-T-C

90823483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15112498-T-G

90823489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15112477-G-T

90823575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15112394-G-A

90823851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15112167-A-G

90823868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15112150-T-A

90823889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15112130-C-T

90824507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15111520-A-G

http://identifiers.org/hco/8/GRCh38#90824584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15111442-C-A

90824584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15111442-C-T

http://identifiers.org/hco/8/GRCh38#90824587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15111439-C-A

90824587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15111439-C-T

90824692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15111323-T-C

90824701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15111313-G-T

90824831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15111186-A-G

90824841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15111175-A-G

90824879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15111137-T-C

90824879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15111137-T-G

http://identifiers.org/hco/8/GRCh38#90824920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15111111-A-C

90824924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15111107-T-G

http://identifiers.org/hco/8/GRCh38#90825109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15111082-C-A

90825270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110922-C-T

http://identifiers.org/hco/8/GRCh38#90825545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15110661-C-A

90825630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110577-G-A

90825736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110475-T-A

90825833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110386-C-G

90825833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110386-C-T

90826074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110255-C-T

90826172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15110157-G-A

90826424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15109919-C-G

90826424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15109919-C-T

90826597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15109753-C-T

90826637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15109721-G-C

90826823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15109568-G-A

http://identifiers.org/hco/8/GRCh38#90827112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15109281-A-C

90827130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15109263-T-C

90828464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108584-A-G

http://identifiers.org/hco/8/GRCh38#90828484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15108564-C-A

90828527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108522-T-C

90828553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108505-A-T

90828819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108352-G-A

90828823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108348-A-G

90828864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108304-A-G

90828929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15108247-A-G

90829420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15107755-G-T

90830131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15107049-A-G

90831282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15105379-A-T

90831296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15105364-A-G

90831340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15105320-T-G

90831415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15105249-C-T

90832248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15102629-G-A

http://identifiers.org/hco/8/GRCh38#90832751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15102160-A-C

90833369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101582-C-T

90833577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101492-C-T

90833744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101338-T-C

90834160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101184-G-A

90834160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101184-G-T

http://identifiers.org/hco/8/GRCh38#90834162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15101182-C-A

90834162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101182-C-T

90834218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101171-T-C

90834293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101113-T-A

90834383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101054-G-A

90834418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15101025-C-T

90834615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15100889-C-G

http://identifiers.org/hco/8/GRCh38#90834750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15100753-A-C

90834899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15100613-A-G

90835133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15100429-G-T

90835346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15100195-A-G

90835362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15100179-T-A

http://identifiers.org/hco/8/GRCh38#90835490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15100053-C-A

90835511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15100032-G-A

90836225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099370-A-G

90836307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099310-C-G

90836450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099159-T-C

90836529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099078-C-G

90836550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099057-A-G

90836575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099036-A-G

90836590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15099021-G-A

90836830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098757-T-C

90837069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098484-T-C

90837163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098391-G-A

90837163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098391-G-T

90837201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098355-C-T

90837219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098337-T-C

90837702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098217-T-C

90837725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15098194-C-T

http://identifiers.org/hco/8/GRCh38#90838013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15097972-C-A

90838013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15097972-C-T

90838928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15097330-C-T

90839051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15097222-T-G

90839064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15097209-G-T

90839416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15096886-T-C

90840389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15094318-G-C

90840425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15094295-G-A

http://identifiers.org/hco/8/GRCh38#90840477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15094272-C-A

90840777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093972-C-T

90840907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093852-A-G

90840946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093815-T-A

90840946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093815-T-C

90841404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093736-G-C

90841505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093641-T-C

http://identifiers.org/hco/8/GRCh38#90841577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15093603-C-A

90841577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093603-C-G

90841620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093562-T-A

http://identifiers.org/hco/8/GRCh38#90842266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15093277-A-C

http://identifiers.org/hco/8/GRCh38#90842279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15093264-C-A

90842491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15093068-T-A

90842600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15092970-A-G

90842783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15092830-T-A

90843551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15092448-T-C

90843565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15092433-C-G

90845615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15091926-T-C

http://identifiers.org/hco/8/GRCh38#90845644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15091911-C-A

90845644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15091911-C-G

90845850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15091182-C-T

90845934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15091095-A-G

http://identifiers.org/hco/8/GRCh38#90845955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15091074-C-A

90846039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15090990-C-T

90846178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15090852-C-T

90846272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15090736-A-G

90849934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15085325-T-C

90862366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15084189-A-G

90862814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083829-T-C

90862841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083802-G-A

90862841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083802-G-T

http://identifiers.org/hco/8/GRCh38#90862897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15083745-A-C

90862929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083714-T-C

90862929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083714-T-G

90862969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083674-T-C

90863080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083582-G-A

90863109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083553-G-A

90863109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083553-G-T

90863141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083527-C-T

http://identifiers.org/hco/8/GRCh38#90863262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15083399-C-A

90863297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083361-T-A

http://identifiers.org/hco/8/GRCh38#90863303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15083355-A-C

90863303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083355-A-G

90863563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15083102-C-T

90863701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082966-A-G

90863758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082911-T-C

90864001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082702-G-A

90864054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082647-T-C

90864121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082581-T-A

90864121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082581-T-C

90864149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082540-G-T

90864182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082503-A-G

90864202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082483-T-C

90864297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082416-A-G

90864331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082385-A-G

90864500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082277-C-T

90864519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082258-C-T

90864557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15082219-A-G

http://identifiers.org/hco/8/GRCh38#90864687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15082070-C-A

90864790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15081983-G-A

90864822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15081954-T-C

http://identifiers.org/hco/8/GRCh38#90864904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15081880-A-C

90865191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15080779-T-A

90867647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15067889-T-A

90867700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15067856-A-G

90870367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15067604-T-C

90870430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15067541-A-G

90870770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15066473-T-G

90870851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15066392-A-G

90870872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15066367-A-G

90871005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15066196-T-A

90871881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15065767-C-G

90872008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15065648-T-C

90872008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15065648-T-G

http://identifiers.org/hco/8/GRCh38#90872049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15065604-C-A

90872049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15065604-C-T

90872150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065325-T-A

90872150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065325-T-C

90872226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065248-T-C

90872280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065197-A-G

90872280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065197-A-T

90872285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065192-T-A

90872285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065192-T-C

90872291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065186-G-A

90872291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065186-G-T

http://identifiers.org/hco/8/GRCh38#90872353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15065111-C-A

90872353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065111-C-T

90872458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15065040-A-G

http://identifiers.org/hco/8/GRCh38#90872607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15064884-C-A

90872727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15064764-A-T

90873171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15064330-T-C

90873181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15064322-C-T

90873904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15063584-C-G

90874219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15063285-T-A

90874219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15063285-T-C

90876389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062851-A-G

90876476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062768-A-G

90876521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062724-G-A

90876672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062614-G-A

90876761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062525-T-G

90876922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062365-A-G

90877240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15062133-A-G

http://identifiers.org/hco/8/GRCh38#90877456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15061911-C-A

90877462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15061902-A-G

90877464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15061900-T-G

90877546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15061818-C-T

90879745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054179-A-T

90879787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15054140-G-A

90880020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15053685-A-G

90880020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15053685-A-T

http://identifiers.org/hco/8/GRCh38#90880257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15053453-C-A

90880763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15052961-A-G

90880924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15052828-A-G

90881340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15052389-C-T

90882373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15047068-C-T

90882642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 15046210-T-C

90883969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15045235-A-G

90884334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15044902-C-G

90885354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15044013-G-A

90885409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15043959-A-T

90885430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15043938-C-T

90885439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15043929-T-A

90885449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15043919-G-A

90885457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 15043911-G-A

90885928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15041427-T-C

90886342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15040988-T-C

90887076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15040161-G-T

90887087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15040150-G-C

90887240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15040012-T-G

90887544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15039435-A-G

90887578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15039399-G-A

90887954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15039005-C-T

90888086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038809-G-A

90888367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15038674-A-G

90888465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15038599-A-G

http://identifiers.org/hco/8/GRCh38#90888484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15038580-C-A

90888502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038561-A-G

90888509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038554-G-A

90891336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038370-T-C

90891493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038232-A-G

90891528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038189-A-G

90891597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15038145-T-G

90892243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15037811-G-A

90892243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15037811-G-T

90892252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15037802-G-A

90892252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15037802-G-C

90892252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15037802-G-T

90892459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15035370-A-G

90892546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15035286-T-C

90893025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15032852-C-G

90893159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15032745-A-G

90893212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15032692-T-A

90893601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15031441-G-A

90893926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15031116-G-T

90894139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030930-G-A

http://identifiers.org/hco/8/GRCh38#90894152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15030928-A-C

90894218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030866-G-A

90894218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030866-G-C

90894287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030794-A-G

90894565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030479-G-T

90894641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030419-A-G

90894657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15030403-T-G

90895183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15029574-A-G

90895323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15029435-G-A

90895346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15029412-T-A

90895381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15029379-A-G

90897422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15028485-A-G

90897442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15028466-G-A

90897456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15028452-G-A

90897487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15028430-T-A

90897699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15028214-T-C

90897808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15028029-A-G

90897998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15027702-T-G

90898247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15027366-A-G

90898302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15027316-A-G

http://identifiers.org/hco/8/GRCh38#90898475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15027179-C-A

90898790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026869-C-T

http://identifiers.org/hco/8/GRCh38#90898865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15026806-C-A

90898899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026769-A-G

90899007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026634-G-C

http://identifiers.org/hco/8/GRCh38#90899148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15026530-C-A

90899148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026530-C-G

90899148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026530-C-T

90899595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026198-G-A

90899668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026134-C-T

90899776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15026035-A-T

90900281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15025308-T-C

90900398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15025168-C-T

90900770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15024838-C-T

90901300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15024321-A-G

90901724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 15023909-G-A

90907669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023879-T-C

90907879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023668-T-C

http://identifiers.org/hco/8/GRCh38#90907897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15023650-A-C

90907897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023650-A-T

90907969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023573-T-C

90908010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023531-C-T

http://identifiers.org/hco/8/GRCh38#90908021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15023520-C-A

90908110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023433-A-G

90908424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15023127-C-T

90908852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15022726-T-C

90908855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15022723-T-G

http://identifiers.org/hco/8/GRCh38#90908889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15022689-A-C

90908992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15022608-C-T

90909108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15022505-G-C

http://identifiers.org/hco/8/GRCh38#90909363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15022241-C-A

90909363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15022241-C-G

http://identifiers.org/hco/8/GRCh38#90909412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15022187-C-A

90909618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15021976-T-C

90909674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15021883-A-G

90909686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15021861-T-C

90909968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15021555-C-T

90910022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15021499-T-A

90911420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15021137-T-C

90911622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15020943-G-C

90912923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013584-C-T

90912932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013575-C-T

90913067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15013431-G-T

90913097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15013401-A-G

90913208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 15013259-T-C

90913271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013242-A-G

90913272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013241-T-C

90913313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15013200-G-A

90914080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15012458-A-T

http://identifiers.org/hco/8/GRCh38#90915099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15009865-A-C

90915188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15009780-A-G

90915441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15009565-A-G

90915519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15009492-G-A

90915563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15009454-A-G

90916304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15006012-A-G

90916313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15006003-T-G

90916345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005971-T-C

90916393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005930-A-T

90916400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005923-A-G

90917100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005443-T-C

90917106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005437-C-T

90917155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005392-T-C

90917285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005296-C-T

90917389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005210-A-G

90917389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005210-A-T

90917468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15005127-T-C

90917525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15005070-G-A

90917669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15004934-T-G

90917689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15004914-T-A

90917689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15004914-T-C

http://identifiers.org/hco/8/GRCh38#90917716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15004886-A-C

90917768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15004845-G-A

90917768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15004845-G-T

90918633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002984-T-C

90918710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002906-G-A

90918948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15004476-T-C

90919635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003832-A-G

90919748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003727-G-T

90919786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003692-A-T

http://identifiers.org/hco/8/GRCh38#90919872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15003609-C-A

90919872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003609-C-T

90920033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003448-A-G

90920150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003332-G-A

90920199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003283-C-T

90920306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003187-T-C

http://identifiers.org/hco/8/GRCh38#90920325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#15003154-A-C

90920383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003100-A-G

90920455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003042-T-C

90920455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15003042-T-G

90920554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002944-T-G

90920591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002906-G-A

90920971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002591-A-G

90921761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002291-C-T

90921990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15002065-C-T

90922156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001904-A-G

90922159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001901-C-T

90922163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001897-T-C

90922268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001795-A-G

90922505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001533-T-C

90922953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001242-T-C

90922967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001215-A-G

90923209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15001001-C-T

90923585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15000670-G-A

90923585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15000670-G-T

90923890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15000014-G-A

90923890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15000014-G-T

90923978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14999926-G-T

90924519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14990351-G-A

90924666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14990218-T-A

90924686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14990201-A-G

90924796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14990096-C-T

90925299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14989521-T-C

90925393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14989417-G-A

90925393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14989417-G-T

http://identifiers.org/hco/8/GRCh38#90925433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14989376-C-A

90925675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14989142-G-T

90925821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14989038-G-A

90925822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14989037-G-C

90925881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14988980-G-C

90925887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14988974-T-C

90925957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14988909-T-A

90926099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14988789-G-C

90926186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14988700-T-A

90926480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14988405-T-C

http://identifiers.org/hco/8/GRCh38#90926704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14988216-A-C

http://identifiers.org/hco/8/GRCh38#90927799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14978674-C-A

90927998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978484-T-C

90928201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978247-T-A

90928201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978247-T-C

90928304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978148-G-A

90928304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978148-G-T

http://identifiers.org/hco/8/GRCh38#90928316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14978075-C-A

90928316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978075-C-G

http://identifiers.org/hco/8/GRCh38#90928331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14978060-C-A

90928331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14978060-C-T

http://identifiers.org/hco/8/GRCh38#90928387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14977981-C-A

90928387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14977981-C-T

90928814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14977673-C-T

90931187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14976875-G-A

90931187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14976875-G-C

http://identifiers.org/hco/8/GRCh38#90931310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14976750-C-A

90931310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14976750-C-T

90931385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14976675-T-C

90931565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14976488-A-G

90933743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975712-T-G

http://identifiers.org/hco/8/GRCh38#90933987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14975487-C-A

90933987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975487-C-T

http://identifiers.org/hco/8/GRCh38#90934044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14975458-C-A

90934044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975458-C-T

90934072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975431-T-A

90934156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975342-T-A

90934287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975201-T-A

90934287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975201-T-C

90934365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 14975122-T-C

http://identifiers.org/hco/8/GRCh38#90934436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14975060-C-A

90934454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14975035-A-T

90934484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14974993-T-C

90934501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14974963-T-C

90936604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14973949-T-G

90936617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14973936-C-T

http://identifiers.org/hco/8/GRCh38#90936732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14973814-C-A

http://identifiers.org/hco/8/GRCh38#90936800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14973746-A-C

90937264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14972860-A-G

90937360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14972761-A-G

http://identifiers.org/hco/8/GRCh38#90937438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14972685-C-A

90937438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14972685-C-T

90937472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14972658-T-A

90940042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14968327-T-C

90940042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14968327-T-G

http://identifiers.org/hco/8/GRCh38#90940069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14968300-C-A

90940069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14968300-C-T

90940094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14968275-T-C

90940306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14966409-A-G

90940560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14966165-T-C

http://identifiers.org/hco/8/GRCh38#90940588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14966137-C-A

90940665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14966081-G-A

90940665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14966081-G-C

90940665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14966081-G-T

90940932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14965850-G-C

http://identifiers.org/hco/8/GRCh38#90940965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14965789-C-A

http://identifiers.org/hco/8/GRCh38#90940972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14965782-C-A

90940972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14965782-C-T

90941137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14965450-G-A

90941513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14965102-C-T

http://identifiers.org/hco/8/GRCh38#90941528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14965087-A-C

90941528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14965087-A-G

90941577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14965041-C-T

90941760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964926-G-A

90941864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964836-G-A

90942016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964710-T-C

90942127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964610-A-G

90942150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964578-G-A

90942205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964525-C-T

90942207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14964523-T-G

http://identifiers.org/hco/8/GRCh38#90942546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14963982-A-C

90943571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14963331-A-T

90943580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14963322-C-G

90943598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14963304-T-A

90944161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14963043-G-A

90944259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14962949-A-G

90944265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14962943-A-G

90944265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14962943-A-T

90944661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14962408-G-C

90944890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14962151-T-C

90948166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14961396-G-C

90948171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14961391-T-C

90948368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14961201-A-G

http://identifiers.org/hco/8/GRCh38#90949662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14960425-A-C

90949679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960408-T-A

90949679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960408-T-C

90949680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960407-G-A

90949680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960407-G-T

http://identifiers.org/hco/8/GRCh38#90949688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14960397-C-A

90949688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960397-C-G

90949711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960374-G-A

90949711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14960374-G-T

http://identifiers.org/hco/8/GRCh38#90949762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14960122-C-A

90949922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14959967-G-A

90949965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14959924-A-T

http://identifiers.org/hco/8/GRCh38#90950015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14959676-C-A

90950015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14959676-C-T

http://identifiers.org/hco/8/GRCh38#90950016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14959675-C-A

90950016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14959675-C-T

90950045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14959652-T-C

90950452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14958592-A-G

90950474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14958569-G-A

http://identifiers.org/hco/8/GRCh38#90950703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14958305-A-C

http://identifiers.org/hco/8/GRCh38#90950945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14958077-C-A

http://identifiers.org/hco/8/GRCh38#90951021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14958005-A-C

90951087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 14957940-G-A

90951189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 14957839-A-G

90951585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14957309-G-A

90952172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 14956820-T-C

90954500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14956415-G-A

90954544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14956377-G-T

90954639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14956288-T-G

90955325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14956055-T-C

90955399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955985-T-A

90955399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955985-T-C

90955427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955970-G-T

90955436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955961-T-C

90955438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955959-G-A

90955438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955959-G-T

http://identifiers.org/hco/8/GRCh38#90955443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14955954-A-C

90955443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955954-A-G

90955443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955954-A-T

90955457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: intron variant
orthologous variants: 14955940-T-C

90955545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 14955858-T-A

90955545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 14955858-T-C

90955545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 14955858-T-G

90955569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955839-A-G

90955594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955814-G-A

90955594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955814-G-T

90955868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955607-T-G

90955960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955318-G-A

90955960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955318-G-T

90956030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955275-A-G

90956030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14955275-A-T

90956536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14954829-C-T

90956694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14954715-A-G

http://identifiers.org/hco/8/GRCh38#90956772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14954649-C-A

90957006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14954512-C-T

http://identifiers.org/hco/8/GRCh38#90957024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14954494-C-A

90957024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14954494-C-T

90957092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14954429-G-T

90957171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14954342-A-G

90957440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14954072-A-G

90957493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14954023-G-A

90957493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14954023-G-T

90957516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14953998-T-C

90957582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14953936-G-A

90957636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 14953908-T-C

http://identifiers.org/hco/8/GRCh38#90957673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14953872-C-A

90957760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953818-A-G

90957760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953818-A-T

90957763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953815-A-G

90957777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953801-G-A

90957777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953801-G-C

90957777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953801-G-T

90957783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953791-T-A

90958022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953560-T-C

90958132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953500-G-A

90958132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953500-G-T

http://identifiers.org/hco/8/GRCh38#90958434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#14953212-C-A

90958565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14953099-C-T

90958708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14952958-G-T

90958747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14952923-A-G

90958747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14952923-A-T

90958925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14952745-T-C

90959004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14952645-A-G

90959004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3 prime UTR variant
orthologous variants: 14952645-A-T

90959184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20983
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 14952479-A-T