186375859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150268469-T-C

186375859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150268469-T-G

186375870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 150268457-G-A

186375975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 150268352-G-T

186376028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268305-T-C

186376028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268305-T-G

186376053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268284-G-A

186376053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268284-G-C

186376053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268284-G-T

http://identifiers.org/hco/1/GRCh38#186376187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#150268144-C-A

186376187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268144-C-T

186376302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150268049-T-C

186378689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150267623-T-A

186378789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150267530-C-G

186378789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150267530-C-T

186378947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150267385-C-T

186379011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150267328-T-A

186379550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150267108-G-A

186379654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150266224-G-A

186379676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150266202-G-C

186379676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150266202-G-T

http://identifiers.org/hco/1/GRCh38#186379734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150266139-C-A

186379734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150266139-C-T

http://identifiers.org/hco/1/GRCh38#186379779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150266090-C-A

186379779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 150266090-C-T

186379839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150266030-A-G

186379972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150265918-G-A

186379972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150265918-G-C

186379972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150265918-G-T

http://identifiers.org/hco/1/GRCh38#186382747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150264649-C-A

186382747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150264649-C-T

http://identifiers.org/hco/1/GRCh38#186382904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150264496-C-A

186382908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150264492-T-C

186383108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 150264320-T-C

186383162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150264266-C-T

186385010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150262872-A-G

186385406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150262816-T-A

186385407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150262815-A-G

186385447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150262790-C-T

186385849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150262427-G-T

http://identifiers.org/hco/1/GRCh38#186385899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150262381-C-A

186385959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150262229-G-T

186386036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150262154-A-G

186386208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150261984-A-G

186386296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150261889-T-C

186386296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150261889-T-G

186387048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150261304-G-A

186387048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150261304-G-T

186387126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150261247-C-T

http://identifiers.org/hco/1/GRCh38#186387140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150261234-A-C

186387585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260769-A-G

186387620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260743-A-G

186388004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260440-T-A

186388004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260440-T-C

186388014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260430-T-G

186388133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260395-T-A

186388421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260305-G-A

186388421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260305-G-T

http://identifiers.org/hco/1/GRCh38#186388431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150260295-C-A

186388431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260295-C-T

186388468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150260258-A-G

186388485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 150260241-G-A

186388485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150260241-G-T

186388596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150260047-A-G

http://identifiers.org/hco/1/GRCh38#186388633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150259993-A-C

186388633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150259993-A-T

186388646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150259989-T-C

186388911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150259595-T-C

186388952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150259539-C-G

186389379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150259037-T-C

http://identifiers.org/hco/1/GRCh38#186389444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150258975-A-C

186389444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258975-A-G

186389444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258975-A-T

186389529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258899-A-G

186389529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258899-A-T

186389540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258892-G-A

186389540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258892-G-C

186389540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258892-G-T

186389699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258738-T-C

186389733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258704-G-A

186389733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258704-G-T

http://identifiers.org/hco/1/GRCh38#186389740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150258697-A-C

186390286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258550-A-G

http://identifiers.org/hco/1/GRCh38#186390299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150258537-A-C

186390305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258533-A-G

186390324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258526-C-G

186390412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258452-G-T

186390540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258319-C-G

186390541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150258318-T-C

186390809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 150258059-T-A

http://identifiers.org/hco/1/GRCh38#186390857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150258011-A-C

186390858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 150258010-G-C

186390907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257961-A-G

186390907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257961-A-T

http://identifiers.org/hco/1/GRCh38#186390947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150257931-A-C

186391221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257748-T-C

186391242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257735-G-A

186391242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257735-G-C

186391327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257659-T-C

186391435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257586-A-G

http://identifiers.org/hco/1/GRCh38#186391447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150257574-A-C

186391447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257574-A-T

186391800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257239-A-G

186391800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257239-A-T

186391818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150257216-A-G

186391921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256989-G-A

186393341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256909-G-A

186393341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256909-G-T

http://identifiers.org/hco/1/GRCh38#186393427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150256823-A-C

186393497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256769-A-G

186393497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256769-A-T

186393591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256687-A-T

186393603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256666-A-G

186393650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256624-C-T

http://identifiers.org/hco/1/GRCh38#186393678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150256598-A-C

186393856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256206-A-T

186393898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256168-T-C

186393938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256135-T-C

186393938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256135-T-G

http://identifiers.org/hco/1/GRCh38#186394059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150256013-C-A

186394059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256013-C-T

186394061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150256011-T-C

186394079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150255995-T-C

186394081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150255993-T-C

186394081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150255993-T-G

http://identifiers.org/hco/1/GRCh38#186394202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150255880-C-A

186394215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150255867-A-T

186396939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150255090-C-T

186397246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150254387-G-A

186398271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150251407-T-C

186398304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 150251382-G-A

186398304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 150251382-G-C

186398563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150251117-T-C

http://identifiers.org/hco/1/GRCh38#186398905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150250693-C-A

http://identifiers.org/hco/1/GRCh38#186398990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150250598-C-A

186398990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150250598-C-G

186398990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150250598-C-T

http://identifiers.org/hco/1/GRCh38#186399091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150250498-A-C

186399091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150250498-A-T

http://identifiers.org/hco/1/GRCh38#186399114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150250475-C-A

186399116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150250473-G-A

186399127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150250462-T-A

http://identifiers.org/hco/1/GRCh38#186399156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150250442-C-A

186399156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150250442-C-T

http://identifiers.org/hco/1/GRCh38#186399198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150250396-C-A

186399198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150250396-C-G

186399198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150250396-C-T

http://identifiers.org/hco/1/GRCh38#186404488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150249019-C-A

186404499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150249008-G-A

186404511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248996-A-G

186404565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248950-C-G

186404639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 150248858-G-A

186404814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248689-T-C

186405949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248034-T-A

186405949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248034-T-C

http://identifiers.org/hco/1/GRCh38#186405950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150248033-C-A

186405950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248033-C-T

186405968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150248019-A-G

186406053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247972-A-G

186406167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150247879-T-C

http://identifiers.org/hco/1/GRCh38#186406179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#150247867-C-A

186406273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247773-T-C

186406273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247773-T-G

186406291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247770-G-C

186406383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247706-A-G

186406451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247600-G-C

186406500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247549-T-C

186406513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247536-G-A

186406547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247502-G-A

http://identifiers.org/hco/1/GRCh38#186406551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150247498-A-C

186406771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247325-A-G

186406810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247297-T-G

186406919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247196-A-T

186407043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247033-A-G

186407059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150247017-T-A

186407517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150246638-A-T

186407747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150246415-C-G

186410574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242720-G-A

http://identifiers.org/hco/1/GRCh38#186411916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150242650-C-A

186411916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242650-C-T

186411929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242633-T-A

http://identifiers.org/hco/1/GRCh38#186412020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150242533-C-A

186412020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242533-C-T

186412069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242486-A-G

186412149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242405-C-T

http://identifiers.org/hco/1/GRCh38#186412399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150242246-C-A

186412404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242241-A-G

186412522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242117-A-G

186412562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242070-A-G

186412563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242069-G-C

186412563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242069-G-T

186412583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150242047-A-G

186412766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241842-C-T

186413057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241605-G-A

186413424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241456-A-G

186413448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241432-A-T

186413478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241401-C-T

186413494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241385-T-A

http://identifiers.org/hco/1/GRCh38#186413509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150241370-A-C

186413552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241334-G-C

186413618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241268-T-C

186413618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241268-T-G

186413645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241242-G-A

186413661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150241228-T-C

http://identifiers.org/hco/1/GRCh38#186415332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150240526-C-A

186415444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150240426-T-C

186415445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150240425-G-C

186415451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150240419-T-C

186417332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239993-G-A

http://identifiers.org/hco/1/GRCh38#186417348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150239973-A-C

186417393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150239926-A-G

186417399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150239920-A-G

186417415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150239907-A-G

186417415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150239907-A-T

186417480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150239392-A-G

186417480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150239392-A-T

186417585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 150239306-A-G

186417602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 150239289-A-G

http://identifiers.org/hco/1/GRCh38#186417642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150239252-C-A

186417686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239214-A-G

186417693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239207-T-C

186418606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239108-T-A

186418606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239108-T-G

186418648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239070-T-A

186418676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150239043-A-G

186418771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150238890-T-C

186418844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150238818-A-G

186419016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 150238630-T-A

186419141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238519-A-T

186419151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238510-T-C

186419151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238510-T-G

http://identifiers.org/hco/1/GRCh38#186419189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150238475-C-A

186419189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238475-C-G

186419189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238475-C-T

186419194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238470-A-G

186419194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 150238470-A-T

http://identifiers.org/hco/1/GRCh38#186419324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150238344-C-A

186419324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238344-C-G

186419345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238323-G-T

186419390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238251-C-G

186419418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238223-A-G

186420139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238136-G-A

186420198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238077-G-A

186420254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238022-T-C

186420260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150238016-A-G

186420327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237954-G-A

186420360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237916-C-T

186420371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237905-G-T

http://identifiers.org/hco/1/GRCh38#186420554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150237720-C-A

186420570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237709-A-G

186420730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237576-A-G

186420768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237568-G-A

186420791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237556-G-T

http://identifiers.org/hco/1/GRCh38#186421045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150237363-C-A

186421045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237363-C-G

186421057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237351-A-G

186421130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237271-A-G

http://identifiers.org/hco/1/GRCh38#186421137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#150237264-C-A

186421250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 150237191-G-T

186421466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24299
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 150236973-G-T