5898825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143951604-G-A

5898936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143951498-G-A

5898936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143951498-G-C

5899012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143951495-A-G

5899013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143951494-G-C

5899013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143951494-G-T

5899141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143951420-G-C

5899196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143951371-T-G

5899421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950749-T-A

5899421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950749-T-C

5899848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950380-A-T

5900043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950189-T-G

5900050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950182-T-C

5900063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950170-C-T

5900194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143950000-A-T

http://identifiers.org/hco/7/GRCh38#5900388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143949803-C-A

5900388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 143949803-C-G

5900388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 143949803-C-T

5900450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143949741-A-G

5900903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143948297-G-A

5900903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143948297-G-C

http://identifiers.org/hco/7/GRCh38#5900925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143948275-A-C

5900925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143948275-A-T

5900935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948265-A-G

5900940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 143948260-G-C

5900965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948242-T-G

5900983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948225-A-G

5900990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948218-T-C

5900996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948212-C-T

http://identifiers.org/hco/7/GRCh38#5901025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143948191-C-A

5901025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948191-C-T

5901090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948128-T-G

5901106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948112-G-A

5901106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948112-G-T

5901108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948110-A-T

http://identifiers.org/hco/7/GRCh38#5901122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143948097-A-C

5901122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948097-A-T

http://identifiers.org/hco/7/GRCh38#5901134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143948085-C-A

5901134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948085-C-G

5901134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948085-C-T

http://identifiers.org/hco/7/GRCh38#5901137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143948082-C-A

5901137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948082-C-G

5901137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143948082-C-T

5901567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947961-T-A

5901567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947961-T-G

5901582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947944-G-A

5901582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947944-G-T

5901598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947928-T-C

5901647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947904-G-A

5901647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947904-G-C

http://identifiers.org/hco/7/GRCh38#5901648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143947903-C-A

5901648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143947903-C-T

5901669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143947882-A-G

5901687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143947864-T-C

5902439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946316-A-G

5902495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946257-A-T

5902523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946226-T-A

5902523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946226-T-C

5902523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946226-T-G

5902545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946201-G-T

http://identifiers.org/hco/7/GRCh38#5902589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143946161-A-C

5902589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143946161-A-G

5902621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143946142-G-A

5902621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143946142-G-C

5902621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143946142-G-T

5902700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143946063-G-C

http://identifiers.org/hco/7/GRCh38#5902767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143945996-A-C

http://identifiers.org/hco/7/GRCh38#5902830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143945349-A-C

5902830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143945349-A-G

5902830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143945349-A-T

5902879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143945300-T-G

http://identifiers.org/hco/7/GRCh38#5904942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143941146-C-A

5904968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941119-G-C

5904968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941119-G-T

5904992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941095-T-G

5905016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941093-A-G

5905038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941083-A-G

5905039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941082-G-T

5905052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941069-T-C

5905052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941069-T-G

5905068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941056-T-C

5905068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941056-T-G

5905071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143941053-A-G

5905262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143940866-C-T

5905275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143940853-T-A

5905275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143940853-T-C

5905367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143940755-G-A

5905367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143940755-G-C

5908905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143939068-T-C

5909053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938940-G-A

5909053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938940-G-T

5909982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938325-A-G

http://identifiers.org/hco/7/GRCh38#5909993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143938314-A-C

5909993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938314-A-G

http://identifiers.org/hco/7/GRCh38#5910003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143938304-A-C

5910003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938304-A-G

http://identifiers.org/hco/7/GRCh38#5910012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143938296-C-A

5910012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938296-C-G

5910012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143938296-C-T

5910123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 143938186-T-C

http://identifiers.org/hco/7/GRCh38#5910159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143938160-A-C

5910228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143938097-G-A

5910228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143938097-G-T

http://identifiers.org/hco/7/GRCh38#5910261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143938063-A-C

5910261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143938063-A-G

5910262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143938062-T-A

5910262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143938062-T-C

5910263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143938061-T-A

5910263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143938061-T-C

5910263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143938061-T-G

5910510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937768-G-A

http://identifiers.org/hco/7/GRCh38#5910518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143937759-A-C

5910518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937759-A-G

5910518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937759-A-T

5910566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937689-T-C

5910572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937683-C-T

5910607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937649-T-A

5910608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937648-G-C

5910616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937640-G-A

5910616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937640-G-T

5910619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937637-C-G

5910619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937637-C-T

http://identifiers.org/hco/7/GRCh38#5910620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143937636-C-A

5910620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143937636-C-G

5911781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935499-G-A

5911781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935499-G-C

5911935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935347-T-C

5911939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935343-T-G

5912730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935193-G-A

5912735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935188-T-C

5912780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143935142-T-C

5913072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934896-C-G

5913072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934896-C-T

5913127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934841-A-G

5913134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934835-T-C

5913199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934773-T-A

5913303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934645-T-C

5913324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934621-G-T

http://identifiers.org/hco/7/GRCh38#5913330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143934613-C-A

5913330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934613-C-G

http://identifiers.org/hco/7/GRCh38#5913333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143934610-A-C

5913333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934610-A-T

http://identifiers.org/hco/7/GRCh38#5913458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143934516-C-A

5913458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934516-C-T

5913622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934338-C-T

5913660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934293-A-G

5913743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934216-G-A

5913937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron variant
orthologous variants: 143934052-C-T

http://identifiers.org/hco/7/GRCh38#5918384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143930685-A-C

5918384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930685-A-G

http://identifiers.org/hco/7/GRCh38#5918425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143930645-C-A

5918494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930617-G-A

5918494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930617-G-T

5918607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930328-G-A

http://identifiers.org/hco/7/GRCh38#5918631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143930299-C-A

5918631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930299-C-T

5918651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930285-G-A

5918651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930285-G-T

5918685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930249-C-G

5918700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143930240-T-C

5918954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929981-T-A

5918954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929981-T-C

http://identifiers.org/hco/7/GRCh38#5919414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143929894-C-A

5919459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929852-G-A

5919551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929755-G-A

5919551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929755-G-C

5919626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929683-G-A

5919626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929683-G-C

5919626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929683-G-T

http://identifiers.org/hco/7/GRCh38#5919629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143929680-C-A

5919629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929680-C-G

5919629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929680-C-T

5919647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929664-G-A

5919647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929664-G-C

5919647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929664-G-T

5919660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929654-T-A

5919660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929654-T-C

5919660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929654-T-G

5919661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929653-T-G

5919734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143929596-G-T

5919881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143929410-A-G

5919980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143929311-T-C

5923552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 143928281-C-G

5923552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 143928281-C-T

http://identifiers.org/hco/7/GRCh38#5923567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143928266-A-C

5923567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143928266-A-G

5923805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143927610-A-G

5923863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 143927553-A-T

5923928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 143927488-G-A

5923928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143927488-G-T

5924167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143926260-G-A

5924167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143926260-G-T

5925679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 143925018-T-C

5925921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 143924780-A-T

5925925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 143924776-G-A

5925925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 143924776-G-T

5926019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143924685-T-A

5926247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143922573-G-A

5926294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143922525-G-A

5926294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143922525-G-C

5926294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143922525-G-T

5926364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143922467-C-G

5926364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3 prime UTR variant
orthologous variants: 143922467-C-T

5926455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 143922354-G-C

http://identifiers.org/hco/7/GRCh38#5926466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143922343-C-A

5926466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143922343-C-T

5926468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143922341-G-A

5926468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143922341-G-T

5926498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143922311-T-C

5926498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143922311-T-G

5926539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 143922276-G-A

5926539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21691
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143922276-G-C