http://identifiers.org/hco/5/GRCh38#147560024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43639690-A-C

147560046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 43639712-A-G

147560046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 43639712-A-T

147560071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: non coding transcript exon variant
orthologous variants: 43639737-C-T

147560113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 43639764-T-C

147560163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43639806-T-A

147560163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43639806-T-C

147560185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43639828-G-A

http://identifiers.org/hco/5/GRCh38#147560190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43639833-C-A

147560190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43639833-C-G

147560240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43639886-G-T

147560284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43639914-G-T

147560328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43639958-C-T

http://identifiers.org/hco/5/GRCh38#147560707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43640286-C-A

147561223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640634-C-T

147561286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640696-G-T

147561329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640738-G-A

147561329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640738-G-C

147561356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640761-G-C

147561356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640761-G-T

147561463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640797-T-A

147561463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640797-T-G

147561552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43640887-T-C

147563377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641163-C-T

147563419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641205-A-G

147563438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641224-T-C

147563442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641228-C-T

147563467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641252-T-G

147563564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641775-G-A

147563564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641775-G-T

147563717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43641908-G-A

http://identifiers.org/hco/5/GRCh38#147563860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43642046-A-C

147563888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642063-G-T

147564216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642379-C-G

147564272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642435-A-T

147564319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642479-C-G

147564319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642479-C-T

147564368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642528-A-G

147564383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642544-A-T

147564546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642713-G-A

147564574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642742-G-A

147564574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43642742-G-C

147564877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643016-A-T

http://identifiers.org/hco/5/GRCh38#147565481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43643339-A-C

147565646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643504-G-A

147565650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643514-T-C

147565761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643626-C-T

http://identifiers.org/hco/5/GRCh38#147565861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43643725-C-A

147566008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643872-T-C

147566087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643939-G-A

147566116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643967-G-A

147566121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643972-T-A

147566121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643972-T-C

147566691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644278-C-T

147567639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43646493-G-T

http://identifiers.org/hco/5/GRCh38#147567810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43646638-C-A

147567810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43646638-C-T

147567857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43646662-A-G

147567905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43646715-C-T

http://identifiers.org/hco/5/GRCh38#147567915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43646725-A-C

147567958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43646767-G-A

147568391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43647474-G-A

147568497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43647577-C-T

http://identifiers.org/hco/5/GRCh38#147568774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43647840-A-C

147568891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43647955-T-A

147568965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648030-T-C

147569004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648060-T-G

147569069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648125-C-T

http://identifiers.org/hco/5/GRCh38#147569310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43648340-C-A

147569364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648403-A-T

http://identifiers.org/hco/5/GRCh38#147569660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43648617-C-A

147569680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648637-A-G

147569680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648637-A-T

147570382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43649223-G-C

147571736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43649831-T-A

147572198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43649979-T-G

147572456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43650200-G-C

147572493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43650237-A-G

147572494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43650238-T-G

147572518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43650260-C-T

147572610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43650345-A-G

147572644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43650379-T-C

147573331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43652603-G-A

147573365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43652634-T-C

147573399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43652659-C-T

147573791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43653653-A-G

http://identifiers.org/hco/5/GRCh38#147574051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43653891-C-A

147574051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43653891-C-T

147574076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43653907-A-T

147574083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43653914-G-C

147574332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654163-C-T

147574370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654197-A-G

147574434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654265-G-A

147574584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654421-T-G

147574599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654436-T-A

147576925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654858-A-T

147576947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654878-A-T

http://identifiers.org/hco/5/GRCh38#147576982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43654907-A-C

147576987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654912-T-A

147577237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655125-A-G

147577423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655389-T-A

147577473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655439-T-C

147577528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655489-T-C

147577682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655655-G-A

http://identifiers.org/hco/5/GRCh38#147577859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43655828-C-A

147577952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655909-A-G

147577974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655931-A-G

147577983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43655940-T-A

147578261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43656223-G-A

147578474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43656447-G-A

147578525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43656500-G-A

http://identifiers.org/hco/5/GRCh38#147578532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43656507-C-A

147578572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43656557-T-G

147578579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43656564-T-G

147578811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43656890-T-A

147578919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43657000-A-G

147578920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43657001-A-G

147584894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43659017-G-C

147584955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43659078-A-G

147585546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659380-C-T

147585604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659438-G-A

147585604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659438-G-T

147585712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659529-A-T

147585959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659776-G-A

147585959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659776-G-T

147585970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659787-A-G

147585970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659787-A-T

147586089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659855-A-G

147586170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659929-T-G

147586174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659933-T-C

147586229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43659977-T-C

147586357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660102-G-C

147586357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660102-G-T

147586566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660310-G-A

http://identifiers.org/hco/5/GRCh38#147586618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43660344-C-A

147586618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660344-C-T

147586666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660388-G-A

147586666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660388-G-T

http://identifiers.org/hco/5/GRCh38#147586925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43660505-C-A

147586925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660505-C-T

147586947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660523-G-A

147586947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43660523-G-T

http://identifiers.org/hco/5/GRCh38#147587206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43660754-C-A

147587388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661047-A-G

147587549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661315-G-T

http://identifiers.org/hco/5/GRCh38#147587677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43661450-C-A

http://identifiers.org/hco/5/GRCh38#147587870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43661654-C-A

147587901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661667-A-G

http://identifiers.org/hco/5/GRCh38#147588178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43661925-A-C

147588185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43661933-T-G

147588358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662084-G-A

147588358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662084-G-T

147588403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662122-G-A

147588403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662122-G-T

http://identifiers.org/hco/5/GRCh38#147588407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43662126-A-C

http://identifiers.org/hco/5/GRCh38#147588507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43662271-C-A

147588617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662377-T-A

147588617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662377-T-G

147588719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662465-T-C

147588901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662652-G-T

147589020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662761-T-C

147589337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662844-C-T

147589491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662917-A-G

147589514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43662940-C-T

147589701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663120-T-A

147590058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663455-G-A

147590058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663455-G-T

147590334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663734-C-T

147590371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663771-C-T

http://identifiers.org/hco/5/GRCh38#147590378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43663778-C-A

http://identifiers.org/hco/5/GRCh38#147590386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43663786-C-A

147590386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663786-C-T

147590431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663831-A-T

http://identifiers.org/hco/5/GRCh38#147590501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43663888-C-A

147590513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43663901-G-T

http://identifiers.org/hco/5/GRCh38#147590801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43664138-C-A

147590801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664138-C-T

147590836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664190-T-C

147590836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664190-T-G

147590890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664245-A-G

147590935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664289-G-A

http://identifiers.org/hco/5/GRCh38#147590972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43664320-C-A

147591183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664506-T-C

147591213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664539-A-G

147591232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43664579-G-T

147592435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43665352-T-C

147592738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43665594-A-G

147592861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43665699-C-T

147592870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43665721-C-G

147592931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43665795-T-C

http://identifiers.org/hco/5/GRCh38#147592934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43665798-C-A

147592977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43665839-G-A

147593082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43666317-C-G

147594057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43666773-C-T

147594078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43666793-A-G

147594277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43666979-A-G

147594582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667181-C-T

147594831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667470-A-G

147594847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667486-A-G

147594918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667555-G-A

147598853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668189-G-A

147598853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668189-G-C

147598878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668214-C-T

147598932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668261-C-T

147599146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668425-T-C

147599238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668515-A-G

147599897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669126-G-C

147599938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669167-A-G

147600025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669227-C-G

147600064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669263-C-T

147600073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669272-A-T

http://identifiers.org/hco/5/GRCh38#147600084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43669283-A-C

147600084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669283-A-T

147600088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669287-T-A

147600088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669287-T-C

147600096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669295-T-C

147600096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669295-T-G

147600100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669299-T-G

147600110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669473-T-G

147600148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669525-C-T

147600159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669536-T-C

http://identifiers.org/hco/5/GRCh38#147600162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43669539-A-C

147600195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669567-T-G

147600384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669745-T-A

147600418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669775-C-T

147600825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670190-T-C

147600962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670316-G-A

147601659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670641-G-A

147601830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670810-A-T

http://identifiers.org/hco/5/GRCh38#147601933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43670905-A-C

http://identifiers.org/hco/5/GRCh38#147601934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43670906-C-A

147601934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670906-C-G

147601934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670906-C-T

147601988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670920-T-C

147601996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670928-T-C

147602395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671310-T-C

147602446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671360-G-A

147602504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671424-T-C

147602571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671481-T-C

147602596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671507-G-C

147602661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671564-T-G

147602662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671565-A-G

147602694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671597-A-T

147603085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672164-T-C

147603358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672394-G-T

147604602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43672955-A-G

147612022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673410-T-G

147612074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673443-G-A

147612074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673443-G-C

147612096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673455-A-G

147612124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673478-T-G

147612162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673519-G-A

147612177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673534-T-C

147612181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673538-G-A

147612181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673538-G-C

http://identifiers.org/hco/5/GRCh38#147612189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43673546-A-C

147612235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673588-T-C

147612453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673789-A-T

http://identifiers.org/hco/5/GRCh38#147612464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43673800-C-A

147612583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43673919-T-C

147612798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674520-A-T

147612825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674551-T-A

147613035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674762-A-G

147613222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674909-G-A

147613222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674909-G-T

147613238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674924-T-A

147613238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674924-T-C

147613241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43674927-A-G

147613412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675085-G-A

147613452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675122-A-T

147613473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675149-T-C

147613523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675199-G-C

147613628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675301-T-C

147613643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675316-G-C

147613643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675316-G-T

http://identifiers.org/hco/5/GRCh38#147613705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43675377-C-A

147613720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675392-C-T

http://identifiers.org/hco/5/GRCh38#147613965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43675592-A-C

147614033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675668-G-A

147614063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675696-A-G

147614073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675706-A-G

147614084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675717-G-T

http://identifiers.org/hco/5/GRCh38#147614086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43675719-A-C

147614134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675766-C-T

147614360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43675998-T-G

147614370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676008-A-G

147614399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676037-G-A

147614706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676476-C-T

147614826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676587-C-G

147614896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676638-G-A

147614937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676679-G-A

147614937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43676679-G-T

http://identifiers.org/hco/5/GRCh38#147615230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43676965-C-A

147615287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677019-G-A

147615491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677185-T-A

147615942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677605-A-G

147615996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677658-G-A

http://identifiers.org/hco/5/GRCh38#147616080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43677738-C-A

147616326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43677979-C-G

147616399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678137-G-A

147616517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678294-T-C

147616581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678352-G-C

147616932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678655-C-T

147616957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678674-C-G

147616957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678674-C-T

147616962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43678679-C-T

147617867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43679965-T-G

http://identifiers.org/hco/5/GRCh38#147618010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43680109-C-A

147618010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43680109-C-T

147618195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680288-T-C

http://identifiers.org/hco/5/GRCh38#147618208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43680301-C-A

147618208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680301-C-G

147618306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43680382-G-T

147619269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681653-G-A

147619352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681734-C-T

147619378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681760-T-C

147619457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681838-T-G

147619496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681877-G-T

147619592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43681957-T-C

147619665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682027-A-G

http://identifiers.org/hco/5/GRCh38#147619800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43682169-C-A

147619898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682267-C-T

147620530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682545-T-C

147620549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682565-A-G

147620577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682593-T-A

147620577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682593-T-C

147620577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682593-T-G

147620763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682778-T-C

147620776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682799-T-C

http://identifiers.org/hco/5/GRCh38#147620800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43682823-A-C

147620800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682823-A-G

147620800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682823-A-T

147620814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682839-A-G

147620837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682858-A-G

147620838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43682859-A-G

http://identifiers.org/hco/5/GRCh38#147620846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43682867-C-A

147621389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43683713-C-T

147621490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43683772-G-T

147621821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684043-G-A

147621821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684043-G-T

147621828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684050-T-C

147621844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43684065-A-G

147623523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685147-T-C

147623559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685181-T-G

147623612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685214-T-C

147623754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685360-C-T

147623803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43685407-G-T

147625495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43686008-A-T

147626233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43686525-G-A

http://identifiers.org/hco/5/GRCh38#147626236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43686528-C-A

147626348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43686632-A-G

147626448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43686723-T-C

147626935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43687152-G-A

147627608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688378-A-G

147627669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688443-G-A

147627669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688443-G-T

147628170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43688998-T-C

147628307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689133-C-T

147628446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689263-G-A

http://identifiers.org/hco/5/GRCh38#147628600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43689409-C-A

147628600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689409-C-G

147628665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689462-G-T

147628728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689523-G-T

147628754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43689549-C-G

147628868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689667-C-T

http://identifiers.org/hco/5/GRCh38#147628870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43689669-A-C

147628870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689669-A-G

147628870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689669-A-T

147628895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689687-T-C

147629122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689843-A-G

147629177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689882-A-G

147629177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43689882-A-T

147629582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43690278-T-C

http://identifiers.org/hco/5/GRCh38#147629584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43690280-A-C

147629634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43690331-G-T

147631156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43690972-G-A

147631156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43690972-G-T

147631305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691111-T-C

147631305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691111-T-G

http://identifiers.org/hco/5/GRCh38#147631329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43691121-C-A

147631329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691121-C-T

147631443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43691235-T-G

http://identifiers.org/hco/5/GRCh38#147631640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43691414-C-A

147631640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691414-C-T

147631653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691427-T-C

147631826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691597-C-T

147632004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691762-A-T

147632208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691916-G-A

147632400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691922-A-G

147632495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43691988-T-C

147632542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43692048-T-C

147632542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43692048-T-G

147632564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43692069-A-G

http://identifiers.org/hco/5/GRCh38#147632877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43692363-C-A

147632934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43692411-G-T

147633032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43692505-T-A

147633182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43692731-T-C

147633434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43693075-T-A

147633513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43693119-G-T

147633559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43693165-G-A

147633996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43693478-T-G

147634090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43693560-A-G

147634093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43693563-A-G

147634777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694675-T-C

http://identifiers.org/hco/5/GRCh38#147634851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43694729-C-A

147634851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694729-C-T

147635216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694905-T-C

147635234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694924-G-C

147635266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694959-T-C

147635292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43694983-A-G

147635466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695148-A-T

147635504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695177-C-T

147635928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695322-T-C

147635951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43695344-C-T

http://identifiers.org/hco/5/GRCh38#147636155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43695533-C-A

147636372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43695746-C-T

http://identifiers.org/hco/5/GRCh38#147636430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43695812-C-A

http://identifiers.org/hco/5/GRCh38#147636593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43695970-A-C

147636756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696131-A-G

147636769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696144-G-C

147636857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696226-T-C

147636919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696289-A-G

147636920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696290-T-C

147636945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696315-G-A

147636989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43696358-T-G

147637127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696503-G-A

147637127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696503-G-C

147637162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696555-G-C

147637162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696555-G-T

http://identifiers.org/hco/5/GRCh38#147637313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43696684-C-A

147637313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696684-C-T

http://identifiers.org/hco/5/GRCh38#147637472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43696804-C-A

147637476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696808-G-C

147637476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696808-G-T

147637479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696811-G-T

147637547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696868-C-T

147637564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696885-C-T

147637575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696895-G-C

147637596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43696916-C-T

http://identifiers.org/hco/5/GRCh38#147638721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43697479-C-A

147638885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43697642-T-C

147639037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697830-G-A

147639258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43697998-G-A

147639381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698186-G-T

147639554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698852-A-G

147639568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698866-A-T

147639580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698878-T-C

147639581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698879-G-A

147639581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698879-G-C

147639581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698879-G-T

http://identifiers.org/hco/5/GRCh38#147639596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43698894-C-A

147639596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698894-C-G

147639596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698894-C-T

147639597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698895-G-A

147639604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698902-C-G

147639611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698908-C-T

147639613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698910-C-G

http://identifiers.org/hco/5/GRCh38#147639872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43699129-C-A

147639872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699129-C-T

147640106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699356-C-T

147640256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699499-G-A

147640674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700126-A-G

147640838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700290-A-G

147640865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700317-G-C

147640865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700317-G-T

147640882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700335-T-C

147640908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700361-G-A

147640908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700361-G-C

147640908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700361-G-T

147640931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700384-A-G

147640931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700384-A-T

147640940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700394-G-T

147640973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700427-G-A

147640973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700427-G-C

147640973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700427-G-T

147641054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700510-T-C

147641160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700615-G-T

http://identifiers.org/hco/5/GRCh38#147641280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43700713-C-A

147641310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43700740-T-C

147641619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701049-T-C

http://identifiers.org/hco/5/GRCh38#147641656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43701086-C-A

147641656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701086-C-T

147641666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701096-G-A

147641666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701096-G-C

147641666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701096-G-T

147641720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43701145-G-A

147641831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701267-G-T

147641833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43701269-C-G

147641872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702433-A-G

147641873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702434-A-G

147642154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702671-A-G

147642227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702749-C-T

147642285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702816-T-A

147642296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702830-T-A

147642299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43702833-T-C

147642611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703106-G-A

147642712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703219-C-T

147642716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703223-T-C

147643185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703244-T-G

147643245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703298-A-G

147643262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703315-G-C

147643623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43703688-A-G

147644033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704097-G-A

147644033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704097-G-C

147644033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704097-G-T

http://identifiers.org/hco/5/GRCh38#147644312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43704366-C-A

147644312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704366-C-T

147644687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704700-C-G

147644701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704713-T-C

147644716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704727-G-T

147644717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704728-G-C

147644717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704728-G-T

147644754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704824-T-C

147644770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704840-G-A

147644770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704840-G-T

147644808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704872-T-C

147644821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43704885-T-A

http://identifiers.org/hco/5/GRCh38#147644913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43704980-C-A

147644976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43705043-G-A

147645067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705135-G-A

147645067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705135-G-C

147645067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705135-G-T

http://identifiers.org/hco/5/GRCh38#147645107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43705160-C-A

http://identifiers.org/hco/5/GRCh38#147645143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43705196-C-A

147646000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43705989-C-T

147646217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706155-A-G

147646603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706528-G-T

147646685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706577-A-G

147646740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706619-A-G

147646839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706707-T-C

147646843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706711-T-C

147646858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706726-A-G

147646979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43706822-T-C

http://identifiers.org/hco/5/GRCh38#147646994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43706837-C-A

http://identifiers.org/hco/5/GRCh38#147647007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43706846-A-C

147648222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708373-T-C

147648261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708412-T-C

147648266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708417-T-G

http://identifiers.org/hco/5/GRCh38#147648353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43708503-C-A

147648353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708503-C-T

147648365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708515-G-A

147648365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708515-G-T

147648499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708649-A-G

147648534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708659-T-C

147648564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708682-T-C

147648901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43708975-G-T

147648918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708997-G-A

147648964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709038-G-A

147649137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709176-T-G

147649139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709178-T-C

147649397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709426-G-C

147649538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709560-G-A

147649556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709578-C-T

http://identifiers.org/hco/5/GRCh38#147649672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43709731-C-A

147649914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709956-A-T

http://identifiers.org/hco/5/GRCh38#147649978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43710014-C-A

147649981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710017-T-C

147650123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710156-G-T

147650206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710223-A-G

147650207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710224-G-T

http://identifiers.org/hco/5/GRCh38#147650208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43710225-C-A

147650222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710239-G-T

147650284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710306-G-A

147650306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710332-T-A

147650307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710333-G-T

147650326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710353-G-A

147650326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710353-G-C

147650326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710353-G-T

147650338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43710365-A-G

147650440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43710467-G-A

147650617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710642-A-G

http://identifiers.org/hco/5/GRCh38#147650645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43710669-C-A

147650645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710669-C-G

147650647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710671-G-A

147650848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711536-C-T

147650903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711592-G-A

147650903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711592-G-T

147651098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711766-C-T

147651126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43711792-C-G

http://identifiers.org/hco/5/GRCh38#147651460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43712140-C-A

147651470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712151-C-T

147651619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712282-A-G

147652044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712552-A-G

147652082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712602-T-A

147652113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712636-T-C

147652232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712758-C-T

http://identifiers.org/hco/5/GRCh38#147652259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43712787-A-C

147652460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712974-G-A

147652484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713173-T-C

147659623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713495-T-C

147659737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43713606-G-A

147659743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713612-G-C

147659785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713654-G-A

147659989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713835-T-A

147659989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713835-T-C

147660125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714143-G-T

http://identifiers.org/hco/5/GRCh38#147660343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43714350-C-A

147660360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714415-A-T

147660376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714429-A-G

147660622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43714649-A-G

147660652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43714675-T-C

147660834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43714830-A-G

147660834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43714830-A-T

147660854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43714851-T-C

http://identifiers.org/hco/5/GRCh38#147661140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43715090-A-C

147661140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43715090-A-G

147661293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 43715243-C-T

147661506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43715456-A-G

147661593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43715574-G-T

http://identifiers.org/hco/5/GRCh38#147661629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43715610-A-C

147661735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43715714-G-A

http://identifiers.org/hco/5/GRCh38#147661828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43715812-C-A

147661828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43715812-C-T

147661954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43715923-T-G

147662047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43715985-T-C

147662047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43715985-T-G

147662354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716280-G-A

http://identifiers.org/hco/5/GRCh38#147662401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43716326-C-A

147662403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716328-G-A

147662418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716344-T-C

147662588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716499-C-T

147662609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716520-G-A

147662687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716610-T-C

147664095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43717269-T-C

147664219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43717398-C-T

147664668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43717828-C-T

147665104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718208-G-A

147665551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718634-T-G

147665710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718969-T-C

147666476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719952-G-C

147666555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720031-G-T

147666558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720034-G-C

147666774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720207-G-C

147666832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720259-A-G

147667051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43720438-C-T

147667142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43720530-C-G

147667159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720547-C-T

147667164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720552-A-G

147667374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720754-C-T

147667481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720849-T-C

147667482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720850-G-T

147667652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721024-C-T

http://identifiers.org/hco/5/GRCh38#147667691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43721082-C-A

147667720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721104-T-C

147667758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721137-G-C

147667844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721217-G-A

147667963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721347-C-T

147667996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721379-A-G

http://identifiers.org/hco/5/GRCh38#147668007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43721390-A-C

147668143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721526-C-G

147668269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721661-A-T

147668271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721663-G-A

147668296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721691-G-A

147668317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721711-C-T

147668555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721940-T-C

147668645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722035-A-G

147668669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722059-A-G

147668763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722150-T-A

147668763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722150-T-C

147668763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722150-T-G

147668863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722240-C-T

147668961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722351-T-C

147668985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722375-T-C

147669055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722440-T-C

147669410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722780-C-T

147669456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722823-G-T

147669510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722877-G-A

147669521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722888-G-T

147669795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722981-C-T

147669852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722998-T-C

147669914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723061-G-T

147669925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723072-T-C

http://identifiers.org/hco/5/GRCh38#147669935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723082-C-A

147669995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723113-T-C

http://identifiers.org/hco/5/GRCh38#147670399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723483-C-A

147670412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723496-T-G

147671610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723547-G-A

147671610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723547-G-T

147671623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723560-G-T

http://identifiers.org/hco/5/GRCh38#147671639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723576-C-A

147671639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723576-C-G

147671639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723576-C-T

147671645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723580-T-C

http://identifiers.org/hco/5/GRCh38#147671652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723587-C-A

147671665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723600-A-G

147671789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43723724-T-C

http://identifiers.org/hco/5/GRCh38#147671900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723834-C-A

147671900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43723834-C-T

147671915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43723852-G-T

147671927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43723864-G-A

147671927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43723864-G-C

147671965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723902-G-A

147671965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723902-G-T

147671968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723905-G-T

147671976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723913-A-G

http://identifiers.org/hco/5/GRCh38#147672002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723939-C-A

147672002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723939-C-T

147672022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723957-T-C

http://identifiers.org/hco/5/GRCh38#147672023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43723958-C-A

147672023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723958-C-G

147672023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723958-C-T

147672027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723962-G-T

147672033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723968-G-A

147672033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723968-G-T

147672051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723985-C-G

147672051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723985-C-T

147672082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724017-T-C

147672082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724017-T-G

http://identifiers.org/hco/5/GRCh38#147672088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43724023-C-A

147672165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724086-C-T

http://identifiers.org/hco/5/GRCh38#147672237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43724143-C-A

147672381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724298-T-C

147672420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724352-A-G

147672430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724362-G-A

147672500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724406-T-C

147672529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724451-G-C

147672534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724456-A-G

147672564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724482-A-G

147672821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724966-C-T

147672875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725019-A-G

147673017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725155-G-A

147673017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725155-G-T

147673338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43725440-T-C

http://identifiers.org/hco/5/GRCh38#147673383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43725483-C-A

147679386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729114-C-T

147679488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729213-C-T

147679595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729329-C-T

147679781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729496-T-A

147679835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43729547-G-A

147680415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730080-A-G

147680429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730094-C-G

147680506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730165-T-C

147680506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730165-T-G

147680530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730189-C-T

147680738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730361-C-T

147681016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730617-G-A

147681160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43730759-A-G

147681345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731155-A-G

147681345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731155-A-T

147681612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731418-G-A

147681612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731418-G-T

http://identifiers.org/hco/5/GRCh38#147681695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43731511-C-A

http://identifiers.org/hco/5/GRCh38#147681762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43731578-C-A

147681762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731578-C-T

147682575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732588-A-G

147682575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732588-A-T

147682891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733039-C-G

147682900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733048-G-A

http://identifiers.org/hco/5/GRCh38#147682976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43733129-C-A

147682979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733132-T-C

147683694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733486-T-C

147683779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733577-G-A

147683779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733577-G-C

147683791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733591-A-T

147683856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733660-G-T

147683934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733747-G-C

147684009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733802-C-G

147684027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733820-T-C

147684358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734082-T-C

147684358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734082-T-G

147684397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734150-T-G

147684463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734211-C-T

147684508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43734251-A-G

147684847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43735974-G-A

147684955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736071-A-G

147684975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736091-A-G

147685091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736212-G-A

147685091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736212-G-C

147685096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736217-T-C

147685381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736483-G-A

147685396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736499-G-C

147685714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736903-T-C

147685731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736920-T-C

147685734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736923-G-A

147685756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736945-G-A

147685761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43736950-T-C

http://identifiers.org/hco/5/GRCh38#147685950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43737117-C-A

147686249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737359-T-C

147686272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737378-A-T

147686287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737391-A-G

147686365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737466-C-T

147686378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737479-G-C

147686526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737821-T-C

147686572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43737867-C-T

147686734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738006-G-A

147686819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738092-T-G

147686843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738117-C-G

147686932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738214-A-G

147686951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738233-G-C

147687290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738558-G-A

147687319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738586-T-C

http://identifiers.org/hco/5/GRCh38#147687323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43738590-C-A

147687417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43738677-C-G

147689103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739749-G-A

147689178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739821-G-A

147689244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43739886-G-A

http://identifiers.org/hco/5/GRCh38#147689351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43739988-C-A

http://identifiers.org/hco/5/GRCh38#147689599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43740235-C-A

147689599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740235-C-G

147689599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740235-C-T

147689662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740296-C-T

147689941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740569-G-A

147689944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740572-A-T

147689983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740610-A-T

147690428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740725-T-C

147690666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740923-G-C

147690712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43740952-T-C

147690954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43741160-T-C

http://identifiers.org/hco/5/GRCh38#147691345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43741554-C-A

147691363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43741568-G-C

147691601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744181-G-A

147691665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744245-T-C

http://identifiers.org/hco/5/GRCh38#147691876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43744405-A-C

147691876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744405-A-T

147691948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744463-G-T

147692081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744592-C-G

http://identifiers.org/hco/5/GRCh38#147692353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43744836-C-A

147692353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744836-C-G

147692368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744851-G-A

147692429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43744913-C-G

147692612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745065-G-T

http://identifiers.org/hco/5/GRCh38#147692652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43745098-C-A

147692652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745098-C-T

147692670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745116-G-A

147692685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745134-T-C

147692805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745267-C-T

147692822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745291-G-T

http://identifiers.org/hco/5/GRCh38#147692838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43745307-A-C

147692838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745307-A-G

147692983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43745449-G-A

147693000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43750940-T-C

147693022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43750963-A-G

147693052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43750993-G-A

147693109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751052-A-G

147693215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751118-C-T

147693233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751136-C-T

147693255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751154-C-T

147693377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751251-T-G

147693419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751294-T-C

147693437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751311-C-G

147693568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751442-A-G

http://identifiers.org/hco/5/GRCh38#147693571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#43751445-C-A

147693571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751445-C-T

147693593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751466-C-T

147693594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751467-T-C

147693648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43751524-T-C

147693752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43752023-C-T

147693783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43752053-C-T

147694580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43752742-C-T

147694715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43752866-T-G