95326545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001724-T-A

95326682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001580-G-A

95326682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001580-G-T

95326791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001509-G-A

95326791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001509-G-T

http://identifiers.org/hco/15/GRCh38#95326796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#71001504-C-A

95326796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001504-C-T

95326853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001448-A-G

95326889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71001412-G-T

95326980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 71001324-G-A

http://identifiers.org/hco/15/GRCh38#95326985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#71001318-A-C

95327200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71001096-C-G

95327200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71001096-C-T

95327378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000923-C-T

95327383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000918-A-G

95327445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000855-T-G

95327489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000810-A-G

95327541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000770-G-A

95327541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000770-G-T

95327678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000663-G-A

95328020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000349-G-T

95328029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000340-C-T

95328075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000293-T-C

95328126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000263-G-A

http://identifiers.org/hco/15/GRCh38#95328167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#71000198-A-C

95328184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000181-G-A

http://identifiers.org/hco/15/GRCh38#95328229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#71000128-C-A

95328229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71000128-C-T

95328537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999927-C-T

95328728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999780-A-G

95328761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999726-G-C

95328897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999665-A-G

95329322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999218-T-G

95329439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999098-G-A

http://identifiers.org/hco/15/GRCh38#95329442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70999095-C-A

95329442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999095-C-T

95329458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999079-G-A

95329494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70999043-G-A

95329936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70998625-T-C

95330376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70998249-A-G

95330556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70998067-A-G

95330563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70998060-T-C

http://identifiers.org/hco/15/GRCh38#95330637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70997986-C-A

95330759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997876-C-G

95330767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997868-G-T

http://identifiers.org/hco/15/GRCh38#95331015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70997653-C-A

95331020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997648-T-C

95331132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997536-A-G

95331413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997261-G-A

95331413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997261-G-T

95331476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997219-C-T

95331838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70997079-A-G

95335715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993763-T-A

95336068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993714-A-G

95336070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993712-G-C

95336154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993648-C-G

95336199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993612-C-T

95336231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993599-A-G

95336248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993582-T-C

95336384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993449-T-C

95336747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70993095-A-G

95336896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992939-G-A

95336896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992939-G-C

95336896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992939-G-T

95336931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992899-G-A

95336931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992899-G-T

95336972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992857-G-A

95337039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992790-C-G

95337039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992790-C-T

95337139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992693-G-A

95337338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992473-G-C

95337338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992473-G-T

95337344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70992467-T-A

http://identifiers.org/hco/15/GRCh38#95337539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70991929-C-A

http://identifiers.org/hco/15/GRCh38#95337571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70991877-A-C

95337737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70991752-T-C

95337797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70991692-T-C

95339096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70990083-A-T

http://identifiers.org/hco/15/GRCh38#95339125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70990054-C-A

95339230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989979-G-T

95339350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989895-A-G

95339396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989842-A-G

95339550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989668-T-A

95339614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989627-C-T

95339651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989594-C-T

95339702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989520-C-G

95339785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989432-G-C

95339785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989432-G-T

95339825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989392-C-G

95339887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989336-G-A

95340050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989213-T-C

95340090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989178-G-A

95340304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989106-C-G

http://identifiers.org/hco/15/GRCh38#95340365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70989056-A-C

http://identifiers.org/hco/15/GRCh38#95340383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70989038-C-A

95340383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989038-C-T

95340392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70989029-A-G

95340954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70988553-A-G

http://identifiers.org/hco/15/GRCh38#95341105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70988403-A-C

95341577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70988258-T-G

95341697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70988138-T-G

http://identifiers.org/hco/15/GRCh38#95342356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70987917-C-A

95342521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987746-G-A

95342521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987746-G-T

95342534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987728-G-A

95342534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987728-G-T

95342568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987694-T-G

95342576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987686-C-T

95342598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987658-A-G

95342605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987651-T-C

95342649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987607-C-T

95342650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987606-A-G

http://identifiers.org/hco/15/GRCh38#95343196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70987103-C-A

95343284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70987030-G-C

95344015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986583-G-A

95344019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986579-T-G

http://identifiers.org/hco/15/GRCh38#95344363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70986191-A-C

95344420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986136-G-A

95344445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986112-G-T

95344474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986083-T-G

95344501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986057-C-G

95344501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70986057-C-T

95344636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985925-T-C

95344648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985913-T-A

95344648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985913-T-C

95344671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985890-G-C

95344677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985884-A-T

95344678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985883-T-A

95344678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985883-T-C

95344716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985846-T-C

http://identifiers.org/hco/15/GRCh38#95344856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70985707-C-A

95344921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985643-G-A

95345041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985537-G-A

95345071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985508-A-G

95345072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985507-A-G

95345282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985296-A-G

95345282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985296-A-T

95345388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985207-C-T

95345464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70985133-G-A

95345590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70985021-G-C

http://identifiers.org/hco/15/GRCh38#95345660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70984958-C-A

95345937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984704-T-A

95346068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984574-T-C

95346234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984445-A-G

95346275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984407-T-C

95346309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984374-T-C

95346311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984372-G-A

95346320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984340-C-T

95346349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984311-A-G

95346409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984263-A-G

95346447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984227-A-T

http://identifiers.org/hco/15/GRCh38#95346475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70984214-A-C

95346475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984214-A-G

95346602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70984079-C-T

95346736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983968-T-C

95346800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983890-A-T

95346891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983807-G-A

95347016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983497-C-G

95347027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983486-T-C

95347194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983326-A-G

95347229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983291-T-C

95347298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983231-G-A

95347333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983194-A-G

95347461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983069-T-C

http://identifiers.org/hco/15/GRCh38#95347483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70983047-A-C

95347508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70983019-G-C

95347538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70982988-A-G

95347542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70982984-G-C

95347677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70982838-G-A

95347677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70982838-G-C

95347773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70982744-T-A

95347852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70982199-T-G

95348122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70981972-C-G

95348181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70981922-G-T

http://identifiers.org/hco/15/GRCh38#95348189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70981914-A-C

http://identifiers.org/hco/15/GRCh38#95348345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70981766-C-A

95348397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70981756-C-T

95348644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70981542-T-G

95348698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70981505-G-A

95348730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70981471-T-C

95349335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980859-A-T

95349341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980853-T-C

95349363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980831-T-C

95349464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980736-G-A

95349558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980672-A-G

95349698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980607-C-T

95349716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980589-T-A

95349929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980419-C-T

http://identifiers.org/hco/15/GRCh38#95349969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70980380-A-C

95350004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980346-C-G

95350022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980331-C-T

95350104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980280-A-G

95350250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70980107-G-T

95350970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70977139-G-A

95351050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70977061-C-T

95351101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70977010-A-G

95352044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70975482-C-T

95352244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70975282-A-G

95352250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70975276-A-G

95352497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70975025-C-T

95352560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974966-C-T

95352564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974962-G-A

95352566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974960-T-G

95353385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974128-T-C

95353462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974052-G-A

95353481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974033-G-C

95353504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70974009-C-T

95353544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973969-C-T

95353780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973749-T-C

95353842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973675-T-C

95353997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973508-G-C

95354001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973500-C-T

95354148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973339-A-G

95354300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973221-T-G

95354310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973211-G-A

95354310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973211-G-T

95354394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973166-T-C

95354490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70973094-C-T

95354789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70972454-T-C

95354813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70972428-A-T

95354926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70972286-A-G

95354981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70972259-G-C

95355071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70972169-A-G

http://identifiers.org/hco/15/GRCh38#95355107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70972133-A-C

95356823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70969318-G-A

http://identifiers.org/hco/15/GRCh38#95357311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70968639-A-C

95357545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70968554-T-C

95357700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70968425-A-T

95358337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70968088-G-A

95358337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70968088-G-C

95359446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70967453-C-T

95359564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70967353-A-G

95359744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70967180-T-C

95359842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70967062-A-T

95359856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70967049-C-T

http://identifiers.org/hco/15/GRCh38#95359986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70966918-C-A

95359986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70966918-C-T

95360016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70966885-G-A

95360016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70966885-G-T

95360496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70966387-C-T

http://identifiers.org/hco/15/GRCh38#95360564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70966325-C-A

95361488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70965224-A-G

95361605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70965055-C-T

95361820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964854-G-A

95361895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964780-T-C

95361912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964763-C-G

95361924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964751-C-T

95362741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964450-T-C

95362783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964413-T-C

95362903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70964286-T-C

95363488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70963676-C-G

95363664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70963508-G-T

95363807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70963385-C-T

95364016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70963172-G-T

95364318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962872-G-T

http://identifiers.org/hco/15/GRCh38#95364491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70962719-C-A

95364538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962673-C-G

95364680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962529-C-T

95364718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962501-A-G

http://identifiers.org/hco/15/GRCh38#95364722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70962497-C-A

95364955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962248-G-A

95365195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962007-G-T

95365199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962003-C-G

95365199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70962003-C-T

http://identifiers.org/hco/15/GRCh38#95366657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70960332-A-C

95366841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70960143-A-T

95366927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70960058-G-A

95366956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70960023-G-C

95366957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70960022-T-G

95366989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959987-G-A

95367114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959854-G-T

95367305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959700-A-T

95367336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959669-T-G

95367379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959634-T-C

95367478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959520-G-A

95367504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959494-C-G

95367699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70959277-A-T

95368303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958912-G-A

95368303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958912-G-C

95368303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958912-G-T

95368374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958842-G-A

95368727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958481-A-T

95368757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958457-A-G

95368761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70958453-G-A

95370373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956831-G-A

95370442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956761-C-T

95370518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956689-C-T

95370634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956580-T-A

95370880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956444-A-G

95370902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956441-G-C

http://identifiers.org/hco/15/GRCh38#95370922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70956419-C-A

http://identifiers.org/hco/15/GRCh38#95370945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70956392-C-A

95371070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70956274-A-G

http://identifiers.org/hco/15/GRCh38#95371684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70953476-C-A

95371684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70953476-C-T

95371912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70953257-C-T

95372003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70953148-T-C

95372179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70952973-T-C

95372434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70952714-T-A

95372455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70952693-A-G

95372775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70952377-T-C

95373125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70951709-T-A

95373293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70951544-A-G

95373371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70951468-A-G

95373744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70951162-G-T

95374122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70950813-A-G

95374227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70950704-T-A

95374227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70950704-T-C

95374262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70950670-G-A

95374815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70950164-A-G

95375086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70949893-G-A

95375350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70949573-A-G

95375472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70949468-C-T

95375571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70949360-A-G

http://identifiers.org/hco/15/GRCh38#95376353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70949016-A-C

95376392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70948979-A-G

95376549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70948824-C-T

95376822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70948579-G-A

95377281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70948118-G-T

95377306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70948093-G-A

95377338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70948060-T-A

95377587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947820-C-T

http://identifiers.org/hco/15/GRCh38#95377879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70947368-A-C

95377956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947337-T-C

95378003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947287-T-A

95378003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947287-T-C

95378003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947287-T-G

95378020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947270-C-T

95378027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947262-T-A

95378059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947234-T-C

95378073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70947220-A-T

95378125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946856-A-G

95378140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946840-C-G

95378140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946840-C-T

95378354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946518-C-T

95378356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946516-G-A

95378356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946516-G-T

95378448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946427-T-C

95378464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946412-T-C

http://identifiers.org/hco/15/GRCh38#95378475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70946401-C-A

95378523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946354-T-G

95378524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946353-A-G

95378635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70946250-G-A

95380832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70943705-A-G

95380865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70943672-G-A

95380999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70943554-G-C

95381120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70943473-A-G

http://identifiers.org/hco/15/GRCh38#95381174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70943439-A-C

95381194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70943421-T-A

http://identifiers.org/hco/15/GRCh38#95381417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70943189-C-A

95381652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942956-T-C

95381826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942629-A-G

95381900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942557-A-G

95381931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942528-C-T

http://identifiers.org/hco/15/GRCh38#95382038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70942435-C-A

95382045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942421-A-G

95382253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942214-G-A

95382261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942206-T-A

95382269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942197-C-T

95382295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942172-G-T

95382355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942115-A-G

95382407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942067-A-G

95382476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70942000-C-T

95382526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70941956-G-A

95382563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70941923-G-T

http://identifiers.org/hco/15/GRCh38#95382564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70941922-C-A

http://identifiers.org/hco/15/GRCh38#95382577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70941902-C-A

95382619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70941859-T-C

95382633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70941845-T-A

95382739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70941500-A-G

95382781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70941458-T-C

http://identifiers.org/hco/15/GRCh38#95383067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70941180-A-C

http://identifiers.org/hco/15/GRCh38#95383197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70941048-A-C

95383392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940834-G-T

95383462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940755-T-C

95383472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940745-T-C

95383599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940621-T-C

95383608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940614-G-A

95383675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940547-A-T

95383847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940407-T-C

95383868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940395-G-A

95383977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940299-G-A

95383989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940287-A-G

95384020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940261-T-C

95384128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940175-G-A

95384157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70940146-A-G

95394041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70939995-T-C

95394113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70939916-C-T

95394297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70939731-G-A

95394382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70939648-C-T

95395098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938944-C-T

95395105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938928-A-G

95395105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938928-A-T

95395115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938895-G-C

http://identifiers.org/hco/15/GRCh38#95395126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70938884-C-A

95395249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938741-C-G

95396136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938193-A-T

95396168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70938161-A-G

95396471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70937927-G-T

95399882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70936179-T-C

95399894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70936167-A-G

http://identifiers.org/hco/15/GRCh38#95399932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70936133-C-A

95399954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70936111-G-A

95400116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70935988-A-G

http://identifiers.org/hco/15/GRCh38#95400947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70934998-C-A

95401284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70934682-G-T

95401551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70934393-G-C

95401767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70934184-T-C

95401788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70934163-A-G

http://identifiers.org/hco/15/GRCh38#95401811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70934141-C-A

95401970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933820-C-T

95402185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933423-T-C

95402230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933369-T-C

95402375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933195-T-A

95402392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933178-G-A

95402410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933160-C-T

http://identifiers.org/hco/15/GRCh38#95402484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70933087-C-A

95402564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933010-T-A

95402564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70933010-T-C

95402615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70932963-C-T

95402823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70932774-C-T

95402951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70932656-G-T

95403140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70932494-C-T

http://identifiers.org/hco/15/GRCh38#95403230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70932411-A-C

95403230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70932411-A-G

95403520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70932155-A-G

95403708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70931966-G-T

95404204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70931494-T-C

95404267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70931432-A-G

95404363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70931342-T-A

95404496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70930944-A-G

95404496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70930944-A-T

95404512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70930928-T-C

95404512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70930928-T-G

95404585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70930858-C-G

http://identifiers.org/hco/15/GRCh38#95404903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70928098-A-C

95404956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70928038-T-A

95404956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70928038-T-C

95405073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927928-T-C

95405355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927670-T-C

95405548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927565-C-G

http://identifiers.org/hco/15/GRCh38#95405553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70927560-A-C

95405597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927518-C-T

95405653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927464-A-G

95405882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927244-T-A

http://identifiers.org/hco/15/GRCh38#95405928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70927194-A-C

95405928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927194-A-G

95405999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927121-A-G

95405999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70927121-A-T

95406690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926657-A-G

95406764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926579-G-A

95406764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926579-G-T

95406765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926578-C-T

95406797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926552-A-G

95406846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926506-T-C

95406883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926467-T-A

95406883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926467-T-C

95407152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926368-C-T

95407185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926335-C-T

95407321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70926194-T-C

http://identifiers.org/hco/15/GRCh38#95407334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70926182-C-A

95407702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70925376-T-G

95407800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70925125-T-C

95407800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70925125-T-G

95408158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70924535-G-C

95408225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70924471-T-C

95408342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70924346-C-T

95409004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70916300-C-T

95409067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70916237-T-C

95409133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70916168-C-G

95409337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70915964-T-A

95409554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70915787-G-A

95409632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70915740-C-T

95409888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70915484-C-T

95409967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70915378-C-T

95410183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70915155-T-C

95410343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70914974-T-C

http://identifiers.org/hco/15/GRCh38#95411434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70914215-A-C

95411583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70914058-A-G

95412236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70913451-T-C

95412353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70913344-T-C

95412518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70913183-G-A

95412945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70912752-T-C

95412980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70912720-C-T

95413037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70912657-G-T

95413043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70912651-G-A

95413043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70912651-G-C

http://identifiers.org/hco/15/GRCh38#95413537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70911855-C-A

95413545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911847-C-T

95413546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911846-C-T

http://identifiers.org/hco/15/GRCh38#95413701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70911698-A-C

95413996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911343-G-A

95414025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70911314-C-T

95416691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70910187-A-G

95416774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70910105-T-A

95417239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70909666-T-C

95417781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908765-T-A

95417781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908765-T-C

95417816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908733-T-C

95417917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908649-C-T

95418025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908542-C-G

95418061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908500-G-A

http://identifiers.org/hco/15/GRCh38#95418449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70908111-A-C

95418486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70908071-T-C

95418591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907801-A-G

95418890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907514-T-A

95418901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907503-A-G

95418975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907434-T-C

95418993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907412-A-G

95419050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907377-C-T

95419205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70907231-T-C

95430146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905879-G-A

95430322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905632-A-G

95430943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70905044-C-T

95431018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904986-G-A

95431069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904937-G-A

95432696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904216-C-T

95432838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70904066-T-C

95432907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70903996-C-T

95433034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70903871-A-G

95433647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70903507-C-T

95433736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902904-G-T

95433782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902863-C-T

95433837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902808-A-G

95433906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902730-T-C

95433971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902671-C-T

95434026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902615-T-C

95434129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902511-T-C

http://identifiers.org/hco/15/GRCh38#95434148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70902492-C-A

95434421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70902038-T-A

http://identifiers.org/hco/15/GRCh38#95434484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70901967-C-A

95438358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901658-A-G

95438358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901658-A-T

95438537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901162-A-G

95438610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901089-A-G

95438624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901080-G-A

95438634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70901070-G-A

95438707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900935-C-T

95438794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900847-A-G

95438794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900847-A-T

95438877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900787-C-T

95438982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900718-C-T

95439177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900647-C-T

http://identifiers.org/hco/15/GRCh38#95439259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70900574-C-A

95439267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900566-G-A

95439267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900566-G-C

95439360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900518-T-C

95439478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900421-C-G

http://identifiers.org/hco/15/GRCh38#95439799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70900303-C-A

95439799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900303-C-T

95439919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900181-T-C

95440019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70900082-T-C

95440272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899829-G-A

95440303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899798-T-A

95440406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899695-T-A

95440464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899634-C-G

95440488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899611-T-C

95440488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70899611-T-G

95441210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70898892-G-A

95441693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70898430-T-A

95441693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70898430-T-G

95441749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70898374-A-G

95442487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897634-T-C

95442801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897295-G-A

95442801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897295-G-T

95442855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897250-G-T

95442888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897221-A-T

95443052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897112-A-T

95443125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70897039-T-A

95443224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896957-T-G

95443258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896932-G-A

95443260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896930-G-A

95443327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896869-A-G

95443544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896667-T-C

95443573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896636-T-C

95443650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896493-C-T

95443742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896387-T-C

95443827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70896291-A-T

95444236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70894185-T-G

95444240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70894181-G-C

http://identifiers.org/hco/15/GRCh38#95444310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70894115-A-C

95444547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70893874-C-T

95447025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70892426-A-G

95447355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70892114-G-A

95447597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891914-C-T

95447619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891892-G-T

95447698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891813-G-C

95447700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891811-G-A

95447700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891811-G-T

95447842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891665-A-G

http://identifiers.org/hco/15/GRCh38#95447844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70891663-A-C

95448031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891491-C-T

95448079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891444-G-A

95448079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891444-G-C

95448108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70891417-T-G

95448302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70890717-T-C

95448666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70890369-A-T

95448946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70890102-A-G

95448972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70890034-G-C

95449600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70889092-A-G

95449803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888897-T-C

95449900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888761-T-G

95449973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888694-C-T

95450062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888609-G-C

95450111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888560-T-G

95450183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888492-G-T

95450246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888391-T-A

95450319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888318-G-A

95450371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70888268-T-C

95450669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887967-G-T

95450690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887946-T-C

95450819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887829-T-C

95450941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887714-A-T

95450949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887706-G-T

95451015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887637-A-G

95451079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887591-A-G

95451138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887540-T-C

95451213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70887454-G-T

95451726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886633-G-T

95452085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886274-G-A

95452137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886222-C-T

95452148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886211-G-A

95452282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886076-T-A

95452282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70886076-T-C

95452397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885968-C-G

95452512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885846-A-G

95452568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885804-C-T

95452572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885800-T-C

http://identifiers.org/hco/15/GRCh38#95452686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70885708-A-C

95452686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885708-A-G

95452765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885633-G-A

95452783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885614-T-C

95452856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885569-A-G

95452905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885521-T-A

95452905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885521-T-C

95453746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885158-A-G

95453746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70885158-A-T

95453758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70885146-T-A

95453840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70885066-A-T

95453867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70885029-T-A

95454187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70884739-C-T

95454392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70884587-G-A

95454423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70884559-T-C

95454454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70884528-A-G

95454529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70884453-A-G

95455376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883611-A-G

95455450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883528-C-T

95455512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883470-C-T

95455525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883457-G-T

95455649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883337-G-T

95455766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70883215-G-A

http://identifiers.org/hco/15/GRCh38#95456214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#70882760-A-C

95456214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70882760-A-G

http://identifiers.org/hco/15/GRCh38#95456545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70882463-C-A

95456547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882461-C-T

95456561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882447-G-A

95456595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882415-T-C

95456708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882292-G-A

95456807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882188-G-A

95456807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882188-G-T

95456817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882178-G-C

95456888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70882131-C-G

95457107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881662-C-G

95457171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881599-G-A

95457250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881454-T-C

95457444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881139-A-G

95457519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70881061-G-A

95457746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880820-T-A

95457757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880809-T-G

95457912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880648-T-G

95457982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880579-G-T

95458064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880496-G-A

95458064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880496-G-T

95458122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880443-C-T

95458209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880352-A-G

95458376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70880191-C-T

95458567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879982-G-C

95458664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879895-C-T

95458739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879821-G-A

95458820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879745-T-A

95458820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879745-T-C

http://identifiers.org/hco/15/GRCh38#95458927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70879644-A-C

95458973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879598-T-G

95459082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879484-G-A

95459082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879484-G-C

95459094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879472-G-A

95459108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879464-A-T

95459171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70879401-T-C

http://identifiers.org/hco/15/GRCh38#95459369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70879230-C-A

http://identifiers.org/hco/15/GRCh38#95459759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70878842-A-C

95459829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878769-C-T

95459895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878697-A-G

95460146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878450-C-T

95460834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878229-A-G

95460976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70878108-A-T

http://identifiers.org/hco/15/GRCh38#95461062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70878012-C-A

95461343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877703-G-A

95461408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877636-G-A

95461408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877636-G-C

95461493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877569-G-A

95461615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877445-T-C

95461663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877397-G-T

95461733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877228-A-G

95461755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70877189-A-G

95461872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70877001-G-A

95461945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70876929-A-G

http://identifiers.org/hco/15/GRCh38#95462953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70875912-C-A

95462953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875912-C-G

95462953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875912-C-T

95462955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875910-C-G

95463193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875646-G-C

95463193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875646-G-T

95463267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875576-C-T

95463317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875481-A-G

95463341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70875457-C-T

http://identifiers.org/hco/15/GRCh38#95463804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70874959-A-C

95464071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70874621-A-G

http://identifiers.org/hco/15/GRCh38#95464089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70874587-C-A

http://identifiers.org/hco/15/GRCh38#95464162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70874529-C-A

95464169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70874520-C-T

95464219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70874468-A-G

http://identifiers.org/hco/15/GRCh38#95464335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70874344-C-A

95465029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873652-T-A

95465094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873585-T-A

95465286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873389-C-T

95465404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873255-C-T

95465607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873071-T-C

95465663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70873004-A-G

95466311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872685-T-C

95466444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872543-A-G

95466550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872446-T-C

95466651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872342-T-C

95466952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872076-T-G

95466971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70872064-T-C

95467082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871939-G-A

95467157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871878-A-G

http://identifiers.org/hco/15/GRCh38#95467573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70871499-A-C

95467573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871499-A-G

95467657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871431-T-C

95467791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871289-A-T

http://identifiers.org/hco/15/GRCh38#95467808-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70871273-A-C

95467884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70871208-C-T

95468130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870774-A-G

95468189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870714-C-G

95468189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870714-C-T

95468255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870649-C-G

95468299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870623-T-G

95468771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870436-G-C

95468823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870392-T-C

95468824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870391-G-A

95468893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870320-T-A

95469213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870027-T-A

95469226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70870014-G-A

95469253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869987-C-T

95469258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70869982-A-G

95470272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70868699-A-T

95470463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70868497-A-G

95470722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867566-G-T

95470823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867440-G-T

95470830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867433-A-G

95471180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867129-C-G

95471180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867129-C-T

95471240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70867069-G-T

95471384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866921-G-T

95471459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866836-G-A

95471929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866353-A-G

95471940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866342-C-T

95472255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866040-A-G

95472255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866040-A-T

95472300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866001-G-A

95472629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865777-T-C

95472753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865654-G-A

95473211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865178-T-C

95473242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865148-C-T

95473396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864994-T-C

95473420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864970-T-G

95473430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864959-G-A

http://identifiers.org/hco/15/GRCh38#95473463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70864926-C-A

95473883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864503-T-A

95473973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864387-G-A

95474049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864311-A-G

95474352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864008-C-T

95474378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863982-C-T

http://identifiers.org/hco/15/GRCh38#95474419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70863939-A-C

95474565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863841-A-G

95474677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863714-A-G

95475415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862633-G-A

95475742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862079-A-G

95475742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862079-A-T

95475756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862051-T-C

95475780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862016-G-C

95475780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862016-G-T

95475784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70862012-G-C

95476705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861155-T-C

95476824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860996-G-A

http://identifiers.org/hco/15/GRCh38#95477081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70860743-A-C

95477081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860743-A-G

95477266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860364-T-C

http://identifiers.org/hco/15/GRCh38#95477291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70860339-A-C

95477291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70860339-A-G

95477909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70859814-G-A

95477916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70859807-T-C

http://identifiers.org/hco/15/GRCh38#95477943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70859783-C-A

95478148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859667-T-A

95478657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858219-C-G

95478662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858214-C-T

95479377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70857165-A-T

95479642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70856881-G-A

95479645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70856878-T-C

95480054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70856467-T-C

95480060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70856461-C-T

95480486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855552-G-A

95480560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855490-G-A

95480939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855149-A-T

95481259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854826-G-T

95481299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854789-G-C

95481313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854775-A-G

95481406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854700-G-T

95481423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854683-T-C

95481492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854421-C-T

95481505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854404-A-G

95481790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853807-T-G

95481796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853801-G-A

95481813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853784-G-C

95481976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853619-C-T

95482090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853512-C-T

95482168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853426-C-T

95482173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853421-A-G

95482228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853370-T-C

95482291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853300-T-A

95482328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853256-A-G

95482331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853253-A-T

95485526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852488-A-G

95485680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852338-T-C

95485728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852290-C-T

95485729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852289-T-A

95486093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851970-T-C

95486154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851904-A-G

95486378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851675-T-C

95486416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851637-C-T

95486553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851500-T-C

95486672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851385-T-C

95486672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851385-T-G

95486727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851329-T-A

95486727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70851329-T-C

95487293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850916-A-G

95487294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850915-T-C

95487350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850849-C-G

95487586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70850493-C-T

95488102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849979-G-A

95488129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849950-G-A

95488129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849950-G-C

95488129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849950-G-T

95488176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849903-T-G

http://identifiers.org/hco/15/GRCh38#95488254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70849827-C-A

http://identifiers.org/hco/15/GRCh38#95488330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70849755-C-A

95488330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849755-C-T

95488348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70849739-G-C

95488884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848677-A-T

95488990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848571-T-C

95489550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70848000-C-T

95489994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70847603-T-G

95490073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70847522-G-A

95491814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70846405-C-T

95491835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70846380-T-C

95492465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845990-A-G

95492558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845893-T-C

95492558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845893-T-G

95492619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845832-T-C

95492622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845829-G-C

95492622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845829-G-T

95492710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845737-G-T

95492721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845726-G-A

95492747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845698-G-A

http://identifiers.org/hco/15/GRCh38#95492974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70845512-A-C

95492977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845509-G-A

95493048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845438-C-T

95493130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845353-G-A

95493439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845162-T-C

95493448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845146-T-C

95493495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845099-G-A

95493495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70845099-G-C

http://identifiers.org/hco/15/GRCh38#95493500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70845094-C-A

95494034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844515-A-G

95494068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844492-G-A

95494080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844480-T-C

95494159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70844396-T-C

95494784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843802-C-T

95495116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843341-C-T

95495118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843339-G-A

95495118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843339-G-T

95495291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70843143-A-G

95495833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842602-A-G

95495903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842544-A-G

95496014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842415-G-A

95496082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842360-G-C

95496091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842351-G-A

95496091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842351-G-T

95496210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842286-T-A

95496328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842169-G-A

95496416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842092-A-G

95496444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842072-A-G

http://identifiers.org/hco/15/GRCh38#95496522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70842007-C-A

95496522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70842007-C-T

95496555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70841974-A-T

95496932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70841150-A-G

95496983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70841105-A-G

95497254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70840879-A-G

95497290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70840843-C-G

95497368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70840738-T-C

95497517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70840526-A-G

95497899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70840080-T-C

95498572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839372-T-A

http://identifiers.org/hco/15/GRCh38#95498645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70839299-C-A

95498646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839298-C-T

http://identifiers.org/hco/15/GRCh38#95498709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70839233-C-A

95498750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839191-T-A

95498774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839167-A-T

95498850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839083-T-A

95498850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70839083-T-C

http://identifiers.org/hco/15/GRCh38#95498915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70839014-A-C

95499198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838587-T-G

95499339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838441-A-T

95499561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838236-A-G

95499581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70838216-C-T

95499901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837931-G-C

http://identifiers.org/hco/15/GRCh38#95499910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70837922-C-A

95499918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837921-T-A

95500160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837663-C-G

95500577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70837250-A-G

http://identifiers.org/hco/15/GRCh38#95501102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70836651-A-C

http://identifiers.org/hco/15/GRCh38#95501154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70836605-A-C

95501212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836584-T-G

95501259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836537-A-T

95501385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70836422-A-G

http://identifiers.org/hco/15/GRCh38#95501397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70836410-A-C

95501532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70836267-T-C

95501617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 70836179-G-A

http://identifiers.org/hco/15/GRCh38#95501790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70836010-C-A

95501884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835934-C-G

http://identifiers.org/hco/15/GRCh38#95502022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70835792-C-A

95502112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835702-G-C

95502125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835689-T-C

95502283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835561-C-T

95502320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835524-A-G

95502406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70835413-A-T

95502853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834807-G-A

95502853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834807-G-T

http://identifiers.org/hco/15/GRCh38#95502874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70834786-C-A

95502943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834694-A-G

95502943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834694-A-T

95503026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834617-G-T

95503206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834431-A-G

95503438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834219-A-G

95503481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70834179-G-A

95504109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833535-G-A

95504109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833535-G-C

95504109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70833535-G-T

95504464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832789-G-C

95504685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70832587-T-C

95505190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70831776-A-G

95506129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70830273-T-C

95506242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70830159-C-T

95506257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70830144-T-C

http://identifiers.org/hco/15/GRCh38#95506260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70830141-C-A

95506260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70830141-C-T

95506401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70830000-G-A

95506401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70830000-G-C

http://identifiers.org/hco/15/GRCh38#95506467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829946-C-A

95506500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829918-G-T

http://identifiers.org/hco/15/GRCh38#95506515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829903-C-A

95506518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829900-G-A

95506743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829660-T-C

95506743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829660-T-G

http://identifiers.org/hco/15/GRCh38#95506774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829606-C-A

95506774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829606-C-G

http://identifiers.org/hco/15/GRCh38#95506792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829579-C-A

95506792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829579-C-T

http://identifiers.org/hco/15/GRCh38#95506858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829498-C-A

http://identifiers.org/hco/15/GRCh38#95506859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829497-A-C

95506859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829497-A-G

95506859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829497-A-T

http://identifiers.org/hco/15/GRCh38#95507330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#70829262-C-A

95507375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829217-G-A

95507378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829214-T-A

95507476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70829124-A-G

95507779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27081
most severe consequence: non coding transcript exon variant
orthologous variants: 70828866-G-T