149730462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61533318-G-A

149730497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61533284-G-A

149730497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61533284-G-T

http://identifiers.org/hco/5/GRCh38#149730665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61533135-C-A

149730716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61533082-T-G

149731596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61532220-T-G

149731742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61532077-C-T

149731778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61532039-C-G

149731879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61531924-C-G

http://identifiers.org/hco/5/GRCh38#149731987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61531813-C-A

http://identifiers.org/hco/5/GRCh38#149732041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61531759-C-A

149732041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61531759-C-G

149732136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61531651-C-G

149732149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61531638-C-T

149732213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61531582-C-G

149733278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61530539-G-A

149733320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61530497-A-G

149733686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61530145-G-T

149733703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61530128-A-G

149733920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61529919-T-A

149734372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61529563-T-A

149734372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61529563-T-G

149734572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61529375-T-C

149735110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61528339-G-A

149735419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61528044-C-T

http://identifiers.org/hco/5/GRCh38#149735661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61527805-C-A

149735661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61527805-C-G

149735661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61527805-C-T

149735727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61527786-A-G

149736398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61527346-A-G

149736609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61527148-A-G

149736931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61526958-A-G

http://identifiers.org/hco/5/GRCh38#149737007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61526867-A-C

149737471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61526339-G-A

http://identifiers.org/hco/5/GRCh38#149737515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61526299-C-A

http://identifiers.org/hco/5/GRCh38#149737554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61526260-C-A

149737554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61526260-C-T

149738464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61524827-G-A

149738523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61524810-C-T

http://identifiers.org/hco/5/GRCh38#149739884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61523953-C-A

149739910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61523924-G-A

149740857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61523019-C-T

149740998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61522845-G-T

149741256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61522595-C-T

149741505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61522344-C-T

149741573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61522269-T-C

149742016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61522172-A-T

149742707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61521431-A-T

http://identifiers.org/hco/5/GRCh38#149743010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61521200-C-A

149743680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61521057-A-G

http://identifiers.org/hco/5/GRCh38#149743740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61521000-C-A

149743740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61521000-C-T

149744628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61520444-C-G

149745269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61520150-T-C

http://identifiers.org/hco/5/GRCh38#149745664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61519723-A-C

149745664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61519723-A-G

149746007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61519205-T-G

149747173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61517243-C-T

149747710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61516738-G-T

149747877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61516551-G-A

149747953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61516482-G-A

149747965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61516470-T-G

149747966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61516469-G-T

149747968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61516467-G-C

149748042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61516396-C-G

149748125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61515974-G-A

149749178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61515006-T-C

http://identifiers.org/hco/5/GRCh38#149749267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61514928-C-A

149749488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61514701-T-G

http://identifiers.org/hco/5/GRCh38#149749519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61514670-C-A

149749600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61514587-A-G

149749628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61514558-A-T

149749747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61514441-C-T

149749756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61514432-G-A

149749756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61514432-G-T

149750211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61513998-C-T

149750654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61513580-G-A

149750654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61513580-G-C

149750809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61513422-C-G

149750825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61513407-C-T

http://identifiers.org/hco/5/GRCh38#149751190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61512862-A-C

149751434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61512486-G-A

149751434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61512486-G-T

149751570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61512357-G-A

149751700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61512228-T-C

149752309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61511591-T-C

http://identifiers.org/hco/5/GRCh38#149754144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61510317-A-C

149754144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61510317-A-T

149754198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61510256-A-T

149754290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61510170-G-A

http://identifiers.org/hco/5/GRCh38#149754378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61510082-C-A

149756836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61508882-G-A

149756942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61508770-C-G

149756992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61508693-C-T

149757099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61508594-G-A

149757463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61507764-C-T

149757799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61507435-C-T

149757970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61507289-G-C

149758146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61507130-C-T

149758500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61506815-A-G

149758653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61506693-A-G

149759035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61505732-C-T

149759040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61505726-A-G

149759600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61505223-G-C

149759600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61505223-G-T

149759712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61505133-C-T

149763485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61502536-G-T

149764380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61502225-A-G

149764646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61501954-G-T

149764647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61501953-G-T

149764841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61501701-A-G

149764956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61501569-C-T

149765892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61501212-T-A

149766791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61500130-C-T

149766799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61500122-C-T

149766982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61499935-C-T

149767236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61499682-G-A

149767308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61499605-G-A

149770988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61498795-T-C

149771051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61498733-C-T

149774127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496937-G-A

149774127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496937-G-T

149774197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496867-T-C

149774231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496834-C-G

149774231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496834-C-T

149774326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496755-C-T

149774436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496653-G-A

149774439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496650-C-T

149774532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496557-G-A

149774532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496557-G-C

149774965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496166-C-T

149775084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496069-G-A

149775098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496055-G-A

http://identifiers.org/hco/5/GRCh38#149775158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61496013-C-A

149775158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61496013-C-T

149775292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61495933-G-A

149775300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61495925-C-T

149775311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61495914-T-C

http://identifiers.org/hco/5/GRCh38#149775545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61495740-C-A

149775843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61495343-T-C

149775925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61495263-C-T

149775986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61495196-A-T

149776203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61494960-C-T

149776521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61494729-C-G

149776770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61494512-A-G

149776907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61494389-T-A

149777273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61494030-C-T

149777522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61493809-T-C

http://identifiers.org/hco/5/GRCh38#149778260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61493379-C-A

149778262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61493377-C-T

149778276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61493368-A-G

149778627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61493051-C-T

149778925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61492799-G-A

http://identifiers.org/hco/5/GRCh38#149778962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61492764-A-C

149779052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61492653-T-G

149779111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61492594-C-T

149779248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61492476-A-G

149779504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61492171-A-T

149779534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61492146-G-A

149779874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61491867-G-C

149780376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61491410-A-T

149780529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61491282-T-C

149780731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61491115-T-C

149780864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61491015-C-T

http://identifiers.org/hco/5/GRCh38#149780895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61490984-C-A

149780895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61490984-C-T

149780901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61490978-C-T

http://identifiers.org/hco/5/GRCh38#149781257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61490929-C-A

149781257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61490929-C-T

149781292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61490893-A-G

149781458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61490707-G-A

149781606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61490607-T-C

149781680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61490525-C-G

149781680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61490525-C-T

149782515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61489462-T-C

149782867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61489130-T-G

149782980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61489019-G-A

149783110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61488930-A-T

149783116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61488924-G-C

149785244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61487657-C-G

http://identifiers.org/hco/5/GRCh38#149785335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61487561-A-C

149785335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61487561-A-G

149785502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61487407-G-A

149785646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61487276-G-A

149787287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61485582-C-G

149787541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61485332-G-A

149789147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61484926-A-T

149789239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61484844-G-A

149789979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61484064-C-T

149790002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61484043-G-C

149790169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483938-G-A

149790439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483731-T-C

149790582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483581-A-G

149790743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483439-C-T

149790887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483328-G-C

149790968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483247-A-G

149791029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61483196-C-T

149791908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61482656-T-C

149791935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61482629-G-C

149791981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61482586-A-G

149792228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61482390-C-T

149793347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61481327-C-T

149793376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61481298-C-G

149793586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61481111-A-G

149793586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61481111-A-T

149793732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61480971-G-A

149794000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61480259-A-G

http://identifiers.org/hco/5/GRCh38#149794754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61479582-A-C

149795186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61478938-C-G

149796122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61478087-T-C

149796156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61478055-T-C

149796177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61478034-G-A

149796419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61477864-A-G

149798543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61476044-C-T

149798716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61475926-G-A

149798771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61475901-C-G

149799006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61475711-G-A

149799482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61475321-A-G

149799503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61475313-C-G

149800349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61474564-G-A

149800612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61473930-C-T

149800614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61473928-C-G

149800636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61473905-G-A

149801395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61473197-T-C

149801395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61473197-T-G

149801674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61472867-C-T

149801702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61472822-G-A

149801799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61472721-G-C

149801803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61472717-C-T

149801987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61472318-C-T

149802384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471995-G-A

149802504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471878-G-A

149802645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471748-T-A

149802645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471748-T-C

149803062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471384-A-G

149803120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471322-C-T

149803143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61471299-A-G

http://identifiers.org/hco/5/GRCh38#149804233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61470443-C-A

149804311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61470383-G-T

149804365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61470343-C-T

149804366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61470342-A-T

149805258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61469728-G-A

149805807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61469290-A-G

149805851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61469246-T-C

149806033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61469044-T-C

149806543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61468616-T-C

149807294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61468031-C-T

149807318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61468009-C-T

149807648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61466592-C-G

149807648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61466592-C-T

149808016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61466223-T-C

149808171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61466101-C-T

http://identifiers.org/hco/5/GRCh38#149808329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61465928-C-A

149808490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61465777-T-A

149808607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61465660-C-T

149810034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61465094-G-A

149810049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61465084-A-T

149810177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464962-T-C

149810244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464895-T-C

149810244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464895-T-G

149810685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464473-C-G

149810812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464348-T-A

http://identifiers.org/hco/5/GRCh38#149810814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61464346-C-A

149810814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464346-C-G

149810834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464323-T-C

149810883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464275-G-A

149810883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464275-G-C

149811003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464199-G-A

149811047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61464151-A-G

149811900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61463444-C-T

149811978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61463373-C-T

149812249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61463175-G-A

149812497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61462880-C-G

149812574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61462801-A-G

149813005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61462435-C-T

149813045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61462391-T-A

149814405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61461841-T-A

http://identifiers.org/hco/5/GRCh38#149814757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61461506-A-C

149814807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61461455-C-T

149814901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61461359-G-A

149814942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61461328-T-C

149815010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61461266-C-T

149815381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61461004-G-A

http://identifiers.org/hco/5/GRCh38#149815382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61461003-A-C

149815408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61460978-A-G

149815415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61460971-A-T

149816047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61460592-G-A

149816244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61460398-T-C

149816904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61459642-C-T

149817119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61459410-T-G

149818270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61458169-G-C

149818361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61458020-A-G

149818392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457999-G-C

149818524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457874-T-A

http://identifiers.org/hco/5/GRCh38#149818752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61457657-A-C

149818752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457657-A-G

149818913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457464-G-A

149818923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457453-A-T

http://identifiers.org/hco/5/GRCh38#149818997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61457383-C-A

149818997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457383-C-G

149818997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457383-C-T

149819076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457309-G-T

149819323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61457073-A-G

149820136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456660-A-G

149820284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456518-G-T

http://identifiers.org/hco/5/GRCh38#149820301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61456501-C-A

149820301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456501-C-T

149820332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456470-T-G

149820409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456401-C-T

149820412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456398-C-T

149820415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456395-T-G

http://identifiers.org/hco/5/GRCh38#149820416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61456394-C-A

149820416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456394-C-G

149820466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61456344-G-A

149820661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456168-A-G

http://identifiers.org/hco/5/GRCh38#149820727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61456128-C-A

149820727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456128-C-G

149820739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456116-G-A

149820739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456116-G-T

http://identifiers.org/hco/5/GRCh38#149820742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61456113-C-A

149820742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61456113-C-T

149820857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61455996-C-T

149821040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61455835-T-C

149821480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454503-C-T

149821481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454502-G-A

http://identifiers.org/hco/5/GRCh38#149821540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61454443-C-A

149821639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454365-G-A

149821755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454242-G-A

149821755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454242-G-C

149821755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454242-G-T

149821795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454207-G-A

149821819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61454183-A-T

http://identifiers.org/hco/5/GRCh38#149822267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61452909-C-A

149822267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61452909-C-T

149822311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61452858-A-G

149822499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61452700-C-G

149822499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61452700-C-T

149822976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61452250-C-T

http://identifiers.org/hco/5/GRCh38#149823251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61452023-C-A

149823251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61452023-C-T

http://identifiers.org/hco/5/GRCh38#149823262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61452012-C-A

149823724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61451525-A-G

149823955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61451362-G-A

149824027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61451305-C-G

149824034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61451298-A-T

149824272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61451101-G-A

149824658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450809-C-T

149824708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450761-G-A

149824723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450746-G-C

149824879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450616-A-G

149824880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450615-A-G

149824882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450613-G-A

149825176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450314-G-A

149825176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61450314-G-T

149825560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449989-G-A

149825598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449958-G-T

149825645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449914-T-G

149825771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449790-G-A

149825797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449772-G-A

149826464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449174-T-C

149826577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449085-G-A

149826577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61449085-G-T

149826787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61448904-T-C

149826857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61448834-C-T

149826874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61448817-G-A

149826874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61448817-G-C

149826892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 61448799-A-G

149826951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448763-G-A

149826951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448763-G-T

http://identifiers.org/hco/5/GRCh38#149826969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61448745-C-A

http://identifiers.org/hco/5/GRCh38#149826994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61448721-C-A

149826994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448721-C-T

149827028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448716-G-A

149827028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448716-G-T

149827033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448711-G-A

149827033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448711-G-T

149827068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448676-A-G

149827254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448532-C-T

149827654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61448108-A-G

149827821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61447938-G-A

149827902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61447869-G-C

149827982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61447802-G-A

149827982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61447802-G-C

149828194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61447622-G-A

149828599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, undefined
orthologous variants: 61447215-C-T

149829382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446683-T-C

149829384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446681-G-C

149829391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446674-G-A

149829571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446494-T-C

149830009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, undefined
orthologous variants: 61446172-T-G

149830051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446141-A-G

149830055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446137-G-A

149830055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446137-G-C

149830055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446137-G-T

149830150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61446003-A-G

149830534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61445483-T-C

149830635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61445417-A-G

149830785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, missense_variant
orthologous variants: 61445321-G-T

http://identifiers.org/hco/5/GRCh38#149830930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61445185-C-A

http://identifiers.org/hco/5/GRCh38#149830984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61445132-C-A

149830984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61445132-C-T

http://identifiers.org/hco/5/GRCh38#149830997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61445123-C-A

http://identifiers.org/hco/5/GRCh38#149830998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61445122-C-A

http://identifiers.org/hco/5/GRCh38#149831004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61445116-C-A

http://identifiers.org/hco/5/GRCh38#149831019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61445099-C-A

149831101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61445012-G-A

149832443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61444767-G-C

149832571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61444662-T-C

149832595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61444638-T-C

149832649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 61444584-T-C

149832847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: synonymous variant
orthologous variants: 61444383-G-A

149832847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61444383-G-C

149832854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61444376-C-G

http://identifiers.org/hco/5/GRCh38#149832906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61444321-C-A

149832906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61444321-C-T

149833230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61444003-G-C

149833259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443974-A-G

149833259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443974-A-T

149833361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443872-G-C

149833496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443734-C-G

149833496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443734-C-T

http://identifiers.org/hco/5/GRCh38#149833517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61443713-C-A

149833517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: synonymous variant
orthologous variants: 61443713-C-T

149833532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443698-G-A

149833640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443608-G-A

http://identifiers.org/hco/5/GRCh38#149833700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61443554-C-A

149833700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443554-C-G

149833700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61443554-C-T

http://identifiers.org/hco/5/GRCh38#149833909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61443378-C-A

149833909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61443378-C-T

149834105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61443238-G-A

149834343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, undefined
orthologous variants: 61443062-G-A

149834448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron_variant, undefined
orthologous variants: 61442958-C-G

149834604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442809-C-T

149834803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442633-A-G

http://identifiers.org/hco/5/GRCh38#149834822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61442613-C-A

149834822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442613-C-T

149834834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442603-T-A

149834834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442603-T-C

http://identifiers.org/hco/5/GRCh38#149835154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61442296-C-A

http://identifiers.org/hco/5/GRCh38#149835169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61442292-C-A

149835200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442265-A-G

149835203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442262-G-A

149835203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61442262-G-T

149835300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: splice acceptor variant
orthologous variants: 61442164-G-C

149835300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: splice acceptor variant
orthologous variants: 61442164-G-T

149835708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441777-C-T

149835711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441774-T-C

149835826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441658-G-T

149836206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441141-G-C

149836206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441141-G-T

149836251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441095-T-C

149836251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61441095-T-G

http://identifiers.org/hco/5/GRCh38#149836295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61441051-C-A

149836433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61440913-G-C

http://identifiers.org/hco/5/GRCh38#149836529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61440817-C-A

149836598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61440748-T-C

149836605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61440741-T-C

149836781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61440568-G-A

149836781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61440568-G-C

149836781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: stop gained
orthologous variants: 61440568-G-T

149836783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: missense variant
orthologous variants: 61440566-G-C

149836885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: synonymous variant
orthologous variants: 61440464-G-A

http://identifiers.org/hco/5/GRCh38#149837125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61440245-C-A

149837207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61440164-T-A

149837432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61440006-T-C

http://identifiers.org/hco/5/GRCh38#149837442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61439996-C-A

149837606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61439830-C-G

149837908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61439426-G-C

149838155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61439284-C-T

149838278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61439174-T-C

149838392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61439097-A-G

149838644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61438911-A-G

149838644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61438911-A-T

149838693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61438872-T-C

http://identifiers.org/hco/5/GRCh38#149839007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61438566-C-A

149839625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61438142-C-T

149839634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61438133-C-T

149839732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61438040-T-C

149839806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61437971-C-T

149840143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61437750-G-A

149840300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61437622-G-A

http://identifiers.org/hco/5/GRCh38#149840509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61437427-A-C

149840509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61437427-A-G

149840514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61437423-C-T

149841010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61436867-G-A

149841061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61436818-A-G

149841153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61436732-T-C

149841323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61436601-A-G

149841341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61436583-G-A

149841418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61436513-G-A

149842061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435972-T-G

http://identifiers.org/hco/5/GRCh38#149842155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435871-C-A

149842155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435871-C-G

http://identifiers.org/hco/5/GRCh38#149842170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435865-C-A

149842170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435865-C-G

149842170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435865-C-T

149842173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435862-G-A

149842173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435862-G-T

149842229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435837-T-G

http://identifiers.org/hco/5/GRCh38#149842241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435824-C-A

149842313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: synonymous variant
orthologous variants: 61435752-C-T

http://identifiers.org/hco/5/GRCh38#149842394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435671-C-A

149842409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435657-G-A

149842409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435657-G-T

149842440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435639-A-G

149842477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435605-A-T

http://identifiers.org/hco/5/GRCh38#149842516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435562-C-A

149842527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435551-A-G

http://identifiers.org/hco/5/GRCh38#149842528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435550-C-A

149842528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435550-C-T

149842735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61435377-A-G

http://identifiers.org/hco/5/GRCh38#149843133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61435235-A-C

149843719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434682-T-G

http://identifiers.org/hco/5/GRCh38#149843748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61434671-C-A

149843967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434388-G-A

149844022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434335-G-A

149844022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434335-G-T

149844075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434242-A-G

149844203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434133-G-A

149844231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61434110-T-C

149844913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61433782-A-T

149845318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61433319-G-A

http://identifiers.org/hco/5/GRCh38#149845500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61433056-C-A

149845500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61433056-C-G

149845500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61433056-C-T

149845534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61433030-G-T

http://identifiers.org/hco/5/GRCh38#149845535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61433029-C-A

149845577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61432984-G-T

http://identifiers.org/hco/5/GRCh38#149845578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61432983-C-A

149845579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61432982-T-G

http://identifiers.org/hco/5/GRCh38#149845596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61432965-C-A

149846057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432522-G-C

149846131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432457-G-A

149846131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432457-G-T

149846170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432418-G-T

149846220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432382-T-C

149846241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432378-T-C

149846241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432378-T-G

149846262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432358-A-T

149847213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432105-C-G

149847226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432091-C-G

149847226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61432091-C-T

149847352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61431942-G-A

149847352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 61431942-G-T

149847791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431445-G-A

149847791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431445-G-T

http://identifiers.org/hco/5/GRCh38#149847806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61431430-A-C

149847806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431430-A-G

149847806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431430-A-T

149847822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431414-G-A

149847822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431414-G-C

149847822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431414-G-T

149847835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431401-C-T

149848130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431088-G-C

149848130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431088-G-T

149848137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431081-A-G

149848154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431064-T-C

149848154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61431064-T-G

http://identifiers.org/hco/5/GRCh38#149848274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61430927-C-A

149848286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430915-G-C

149848286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430915-G-T

http://identifiers.org/hco/5/GRCh38#149848362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61430843-C-A

149848682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430529-T-C

149848683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430528-G-A

149848683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430528-G-T

149848854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430380-G-A

149848932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61430317-G-A

149849339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429919-T-C

149849575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429686-C-G

149849575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429686-C-T

http://identifiers.org/hco/5/GRCh38#149849690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61429576-C-A

149849690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429576-C-T

149849747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429519-A-G

149849791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429480-G-A

149849791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429480-G-T

149849846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429433-G-A

149849846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429433-G-T

149849855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429424-A-T

149849922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429354-T-C

149850202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429081-T-C

149850259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61429040-G-T

149850360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428947-G-T

149850448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428872-A-G

149850451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428869-G-A

149850522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428815-A-G

149850642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428684-G-A

149850655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428671-A-G

http://identifiers.org/hco/5/GRCh38#149850778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61428558-C-A

149850811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428525-T-C

149850841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428495-C-T

149851042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428293-A-G

149851098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61428254-G-A

149851429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427990-G-T

http://identifiers.org/hco/5/GRCh38#149851449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61427970-C-A

149851449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427970-C-G

149851449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427970-C-T

149851493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427930-G-C

149851862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427541-A-G

149851953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427454-A-G

149852032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427381-A-G

149852129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427295-G-T

http://identifiers.org/hco/5/GRCh38#149852186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61427240-C-A

149852249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427207-T-C

149852267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61427189-A-G

http://identifiers.org/hco/5/GRCh38#149852575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61426930-C-A

149852825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61426689-C-G

149853440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61426060-G-A

149853440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61426060-G-T

http://identifiers.org/hco/5/GRCh38#149853478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61426026-C-A

149853871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425625-A-G

149853893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425603-T-C

149853903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425592-T-G

149853959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425540-C-T

149854000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425499-G-A

149854169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425327-G-T

149854230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425266-C-T

http://identifiers.org/hco/5/GRCh38#149854290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61425207-C-A

149854290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425207-C-T

149854306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425188-G-A

149854306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425188-G-T

149854330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425171-G-T

149854332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61425169-T-G

149854598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 61424937-T-C

149855023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61424513-G-C

149855034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61424502-G-A

149855034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61424502-G-T

149855074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61424443-C-T

149855076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30022
most severe consequence: intron variant
orthologous variants: 61424441-C-T