http://identifiers.org/hco/6/GRCh38#154154596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6835666-C-A

154154735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835834-T-A

154154814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835917-T-C

154154814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835917-T-G

154154905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836003-C-T

154155193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836231-T-C

http://identifiers.org/hco/6/GRCh38#154155264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6836296-C-A

154155392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836417-A-G

http://identifiers.org/hco/6/GRCh38#154155449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6836475-C-A

154155449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836475-C-T

154155491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836535-G-T

http://identifiers.org/hco/6/GRCh38#154155600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6836571-C-A

154155909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836665-C-G

154155909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836665-C-T

154156170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836901-T-C

http://identifiers.org/hco/6/GRCh38#154156175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6836906-C-A

154156175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836906-C-T

http://identifiers.org/hco/6/GRCh38#154156177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6836908-C-A

154156220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836949-A-G

http://identifiers.org/hco/6/GRCh38#154156287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6836994-C-A

154156287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6836994-C-T

154156323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837027-G-T

http://identifiers.org/hco/6/GRCh38#154156333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837037-C-A

154156333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837037-C-T

154156352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837056-G-T

http://identifiers.org/hco/6/GRCh38#154156357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837061-C-A

154156357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837061-C-T

154156368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837072-T-C

154156371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837075-G-A

154156371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837075-G-T

http://identifiers.org/hco/6/GRCh38#154156434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837097-C-A

154156434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837097-C-T

154156480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837147-T-C

154156512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837182-A-G

154156512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837182-A-T

154156520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837190-A-G

154156540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837214-A-G

154156546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837229-A-G

154156565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837247-A-G

154156618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837299-A-G

154156734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837411-A-G

http://identifiers.org/hco/6/GRCh38#154156762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837439-C-A

154156775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837446-G-T

http://identifiers.org/hco/6/GRCh38#154156868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837547-C-A

http://identifiers.org/hco/6/GRCh38#154156923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837605-C-A

154156933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837615-G-T

154156940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837622-G-A

154157189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837840-T-C

http://identifiers.org/hco/6/GRCh38#154157206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837873-C-A

154157206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837873-C-G

http://identifiers.org/hco/6/GRCh38#154157292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837955-C-A

154157292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837955-C-T

http://identifiers.org/hco/6/GRCh38#154157298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837961-A-C

154157298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837961-A-G

http://identifiers.org/hco/6/GRCh38#154157317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6837980-C-A

154157317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6837980-C-T

154157378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838044-T-C

http://identifiers.org/hco/6/GRCh38#154157439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6838086-C-A

154157458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838105-T-C

154157496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838148-C-T

154157544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838197-A-G

http://identifiers.org/hco/6/GRCh38#154157682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6838332-C-A

154157686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838336-T-G

154157744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838388-C-G

http://identifiers.org/hco/6/GRCh38#154157825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6838469-A-C

154158036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838659-G-A

154158053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838676-T-G

http://identifiers.org/hco/6/GRCh38#154158269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6838879-C-A

154158300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838910-G-T

154158322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6838927-T-C

154158577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839180-G-A

154158577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839180-G-T

http://identifiers.org/hco/6/GRCh38#154158620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6839245-C-A

154158620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839245-C-T

154158723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839378-G-A

154158723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839378-G-T

154158895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839557-T-C

154159027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839661-G-A

154159036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839670-C-T

154159102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6839731-A-G

http://identifiers.org/hco/6/GRCh38#154159233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6839870-C-A

154159268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6839918-T-C

154159304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6839950-T-C

http://identifiers.org/hco/6/GRCh38#154159356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6839996-C-A

154159356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6839996-C-T

http://identifiers.org/hco/6/GRCh38#154159369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6840009-A-C

154159370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840010-G-T

154159395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840033-G-T

154159673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840323-G-A

154159673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840323-G-T

154159703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840351-A-T

154159708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840356-G-A

154159708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840356-G-C

154159795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840442-T-C

http://identifiers.org/hco/6/GRCh38#154159858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6840505-A-C

154159868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840515-T-C

154159917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6840552-G-A

154160029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6840664-A-G

154160250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6840887-G-C

154160295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6840915-C-T

154160375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841007-C-T

154160431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841061-C-T

154160542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841174-G-T

154160552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841184-T-C

154160647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841259-T-C

154160715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841296-G-A

154160717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841298-G-A

154160771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6841348-T-C

154165429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847582-G-C

154165612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847757-G-C

154165625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847767-G-A

154165637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847779-G-A

154165645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847787-C-T

154165821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6847947-G-C

154165921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848046-T-G

http://identifiers.org/hco/6/GRCh38#154165926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6848051-C-A

154165928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848053-C-T

154166044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848164-A-G

154166329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848469-C-T

154166697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848820-G-T

154166770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848879-G-T

154166870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848975-A-T

154166879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6848982-A-G

154167059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6849161-C-T

154167225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6849314-T-A

154167273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6849362-C-T

http://identifiers.org/hco/6/GRCh38#154167335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6849424-C-A

154167335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6849424-C-T

154167706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850365-C-T

http://identifiers.org/hco/6/GRCh38#154167781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6850429-C-A

154167781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850429-C-T

http://identifiers.org/hco/6/GRCh38#154167844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6850489-C-A

154167844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850489-C-G

154167881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850526-A-G

154167888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850542-T-C

154167891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850545-A-G

154168075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6850725-G-A

154168075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6850725-G-T

154168188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850833-G-A

154168188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850833-G-T

154168211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850854-C-G

http://identifiers.org/hco/6/GRCh38#154168222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6850865-C-A

154168245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850891-G-T

154168256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850902-T-G

154168258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850904-T-C

154168258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6850904-T-G

154169433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6851858-A-G

154169953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852274-A-G

154169962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852280-T-A

http://identifiers.org/hco/6/GRCh38#154170001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6852295-C-A

154170001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852295-C-T

154170012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852306-C-T

154170104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852401-C-T

154170160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852457-G-A

154170292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852595-A-G

154170559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6852865-T-G

154170717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6853367-G-C

154170843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6853497-G-A

154170843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6853497-G-T

154178584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6857059-A-G

http://identifiers.org/hco/6/GRCh38#154178899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6857368-A-C

154178904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6857373-C-G

154178977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6857436-G-A

154178984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6857443-T-C

154179024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6857483-G-A

154179261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6857778-G-A

154179347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6858095-T-A

154179411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6858162-A-G

154179510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6858258-T-G

154179651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6858378-T-C

154179776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6858496-G-A

154179880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6858599-T-G

154180237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6859395-G-A

154180460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6859796-A-G

154180528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6859863-T-C

154180593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6859932-A-G

154180616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6859955-G-A

154180991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6860326-T-C

154181001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6860335-G-C

154181133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6860432-A-G

154181227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6860518-T-C

154193685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864302-C-G

154193695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864313-G-A

154193724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864341-C-G

154193724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864341-C-T

154193822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864436-T-C

154194210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864597-A-G

154194365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6864837-C-T

154194629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865103-C-G

154194712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865187-T-C

154194861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865334-T-C

154195017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865502-A-T

154195113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865571-G-C

154195113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865571-G-T

154195555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865697-C-G

154195579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6865720-C-T

154196761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6866137-T-C

154196842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6866226-T-G

154197301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6866690-T-C

154197351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6866740-T-A

154197757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867139-T-C

154197798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867180-T-C

http://identifiers.org/hco/6/GRCh38#154198105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6867907-A-C

154198122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6867925-G-C

154198928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6869045-C-T

154198968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6869086-A-G

154199074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6869184-A-G

154199387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6869431-T-C

154199388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6869432-T-C

154199861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6869907-T-C

http://identifiers.org/hco/6/GRCh38#154200100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6870154-C-A

http://identifiers.org/hco/6/GRCh38#154200129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6870183-C-A

154200172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870238-G-A

154200172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870238-G-C

154200172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870238-G-T

154200173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870239-G-A

154200212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870278-G-A

154200266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870330-T-A

154200266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870330-T-G

154200333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6870405-T-G

154201267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6874356-C-T

154201384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6874455-C-T

http://identifiers.org/hco/6/GRCh38#154201502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6874563-C-A

154201502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6874563-C-T

154201554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6874615-G-A

154201975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6875045-T-A

154202014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6875086-G-A

154202164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6875197-C-T

154202373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6875334-A-G

http://identifiers.org/hco/6/GRCh38#154202473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6875433-A-C

154202507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6875466-T-G

154202868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876349-A-T

154202908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876389-G-A

154203047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876532-T-C

154203105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876589-T-C

154203174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876642-C-T

154203241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876707-A-G

http://identifiers.org/hco/6/GRCh38#154203276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6876741-A-C

154203329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6876792-T-G

154203986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6877153-T-A

154203990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6877158-A-G

154204241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6877641-T-C

154206083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6878396-C-G

http://identifiers.org/hco/6/GRCh38#154206941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6880347-C-A

154206998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880436-G-C

154207143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880585-T-C

154207239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880653-T-G

154207269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880684-G-A

154207269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880684-G-T

154207441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880895-T-C

154207475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6880929-C-T

154207890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6881222-T-C

http://identifiers.org/hco/6/GRCh38#154208117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6881379-C-A

http://identifiers.org/hco/6/GRCh38#154208172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6881452-C-A

154208172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6881452-C-T

154208275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6881542-C-T

154208730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6881967-T-C

154209085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6882591-C-T

154209205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6882725-A-T

154209356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6882868-G-A

154209690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6882908-G-T

154209938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6883754-C-T

154209948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6883764-A-T

154211866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6884192-C-G

154212026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6884373-C-T

154212294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6884701-C-T

154212393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6884800-A-G

154212520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6884927-C-T

154212909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885329-T-C

154213002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885493-G-A

154213002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885493-G-T

154213005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885496-G-T

154213064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885556-G-T

154213098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885590-G-T

http://identifiers.org/hco/6/GRCh38#154213139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6885631-C-A

154213139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885631-C-G

154213157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885639-C-T

154213204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885679-A-G

154213204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885679-A-T

154213218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885691-A-T

154213269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885749-A-G

154213270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885750-G-A

154213270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885750-G-T

154213317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885797-A-G

154213318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6885798-C-T

154213450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6886355-G-C

http://identifiers.org/hco/6/GRCh38#154213681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6886571-C-A

154213681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6886571-C-T

154213764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6886658-C-G

154213764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6886658-C-T

154213919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6886805-T-C

154214118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6886996-A-G

154214168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887050-C-G

154214168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887050-C-T

154214289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887172-T-C

154214326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887210-C-G

154214326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887210-C-T

http://identifiers.org/hco/6/GRCh38#154214372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6887275-C-A

154214420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887316-G-A

154214420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887316-G-T

http://identifiers.org/hco/6/GRCh38#154214434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6887330-C-A

154214434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887330-C-T

154214451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887347-T-C

154214499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887392-A-G

154214518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6887410-G-A

http://identifiers.org/hco/6/GRCh38#154214665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6887640-A-C

154215882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6888291-G-A

154216130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6888489-T-C

http://identifiers.org/hco/6/GRCh38#154219116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6902909-C-A

154219152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6902959-G-A

154219152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6902959-G-T

154219166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6902965-A-G

154219166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6902965-A-T

154219167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6902966-A-G

154219167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6902966-A-T

154219322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903113-G-A

154219322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903113-G-T

154219372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903163-G-A

154219474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903250-A-G

154219618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903405-G-A

154219669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903453-G-A

154219941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903733-G-A

154220097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903848-G-A

154220224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6903988-T-C

154220825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904230-G-A

154220870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904280-G-A

154220932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904336-G-A

154221016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904420-C-T

154221028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904432-C-T

154221100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904499-G-T

154221111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904513-G-A

154221111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904513-G-T

154221180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904596-T-C

154221259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 6904672-G-A

154221461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6904789-G-T

154222089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905102-C-G

154222089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905102-C-T

154222191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905203-T-C

http://identifiers.org/hco/6/GRCh38#154222234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6905236-C-A

154222234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905236-C-T

154222629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905616-G-A

http://identifiers.org/hco/6/GRCh38#154222728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6905703-A-C

154222731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905706-T-C

154222769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905735-C-T

http://identifiers.org/hco/6/GRCh38#154222811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6905773-C-A

154222811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6905773-C-T

http://identifiers.org/hco/6/GRCh38#154223078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6905964-C-A

154223106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6905992-G-A

154223106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6905992-G-T

154223154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6906043-A-T

154223155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6906044-T-C

154223155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6906044-T-G

154223214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6906103-C-T

http://identifiers.org/hco/6/GRCh38#154223250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6906139-C-A

154223266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906151-A-G

154223318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906192-G-T

154223329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906203-G-A

154223329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906203-G-T

154223395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906260-G-A

154223395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906260-G-C

154223395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906260-G-T

154223478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906397-G-T

154223486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906405-A-T

http://identifiers.org/hco/6/GRCh38#154223508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6906427-A-C

154223633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6906563-G-A

154223944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907015-T-C

154223984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907104-T-C

154224054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907174-A-G

154224061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907181-G-A

154224061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907181-G-T

154224075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907195-T-C

http://identifiers.org/hco/6/GRCh38#154224078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6907198-A-C

154224095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907215-A-G

154224142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907262-A-G

154224211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907330-G-A

154224211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907330-G-C

154224324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6907454-G-T

154227868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6913596-T-C

154228067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6913823-T-C

http://identifiers.org/hco/6/GRCh38#154228319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6914054-A-C

154228354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6914089-T-C

154228981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6914655-C-T

154229018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6914692-G-A

154229251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6914876-T-A

154229942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6915292-C-T

154229970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6915311-G-A

154230056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6915377-T-C

154230081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6915401-G-A

154233488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6918265-G-T

154233761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6918551-C-T

154233784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6918574-C-T

http://identifiers.org/hco/6/GRCh38#154234576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6919290-C-A

154234596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919310-C-T

154234600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919314-C-T

154234611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919325-A-G

http://identifiers.org/hco/6/GRCh38#154234812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6919444-C-A

154234837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919463-T-C

154234872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919499-A-T

154235099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919739-T-C

154235142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6919783-T-C

http://identifiers.org/hco/6/GRCh38#154235617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6921032-C-A

154235617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6921032-C-T

154236136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6921541-G-A

154236350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6921782-C-T

154236456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6921885-T-C

154236487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6921913-A-G

154236650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6922101-G-T

154236744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6922204-G-C

154236768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6922230-T-C

154236837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6922255-T-C

http://identifiers.org/hco/6/GRCh38#154236903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6922295-C-A

http://identifiers.org/hco/6/GRCh38#154237069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6922439-A-C

154237328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6922689-T-A

http://identifiers.org/hco/6/GRCh38#154237410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6922746-C-A

http://identifiers.org/hco/6/GRCh38#154237478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6922811-C-A

154237537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6922885-A-T

http://identifiers.org/hco/6/GRCh38#154237837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6923077-A-C

http://identifiers.org/hco/6/GRCh38#154237847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6923087-C-A

154237854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6923094-A-G

http://identifiers.org/hco/6/GRCh38#154237968-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6923164-A-C

154240129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6923463-G-T

154240205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6923508-T-C

154240237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6923547-G-A

154240474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6924272-T-C

154240534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6924329-G-A

154240610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6924399-T-A

http://identifiers.org/hco/6/GRCh38#154240656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6924443-C-A

http://identifiers.org/hco/6/GRCh38#154240742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6924532-C-A

154241046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6924775-G-A

154241608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925028-C-G

http://identifiers.org/hco/6/GRCh38#154241684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6925107-A-C

154241796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925199-T-A

154241932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925323-A-G

154242045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925434-C-T

154242107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925489-G-A

154242368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925737-C-T

154242487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6925845-A-T

154243038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6926061-G-A

154243419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6926432-G-T

154243599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6926597-T-A

154244224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6927527-G-A

154244528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6927781-G-A

154244763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6928024-G-A

154244923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6928168-T-A

http://identifiers.org/hco/6/GRCh38#154245869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6928795-A-C

154245869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6928795-A-T

154245940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6928853-G-A

154245940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6928853-G-C

http://identifiers.org/hco/6/GRCh38#154246090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6928991-C-A

154246321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929250-C-T

154246370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929303-C-G

154246451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929381-T-A

http://identifiers.org/hco/6/GRCh38#154246501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6929432-C-A

154246501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929432-C-T

http://identifiers.org/hco/6/GRCh38#154246515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6929439-C-A

154246515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929439-C-T

154246529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929453-T-C

http://identifiers.org/hco/6/GRCh38#154246546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6929475-C-A

154246546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929475-C-G

154246546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929475-C-T

154246775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929698-T-G

154246825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929718-T-C

154246872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6929765-G-A

154246900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929787-T-A

154246900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6929787-T-G

http://identifiers.org/hco/6/GRCh38#154247625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6930429-C-A

154247625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 6930429-C-G

154247625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 6930429-C-T

154247711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6930510-G-A

154247711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6930510-G-T

154247726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6930523-G-A

154247726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6930523-G-T

http://identifiers.org/hco/6/GRCh38#154248001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6930768-A-C

154248061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6930804-T-C

154248616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6931337-G-A

154248616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6931337-G-C

154249093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6932084-G-A

154249143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6932124-G-T

154249482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6932437-C-G

154249678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6932637-C-T

154249791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6932761-A-G

154250814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 6934135-G-T

http://identifiers.org/hco/6/GRCh38#154250898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6934226-C-A

154253696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6935201-T-A

154253696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6935201-T-G

154257155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936422-G-T

154257166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936431-T-C

154257352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936606-C-G

154257352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936606-C-T

154257425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936679-A-G

154257494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936747-T-A

154257494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936747-T-C

154257867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6936928-T-G

154258717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6937622-A-G

154258744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6937649-G-C

154258803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6937701-G-C

154258941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6937846-A-G

154259041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6937956-C-T

154259266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6938179-A-G

154260066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6938666-G-C

154260376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6938994-T-G

154260474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939046-A-G

154260496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939068-G-T

154260498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939070-A-G

154260498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939070-A-T

154260509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939081-A-G

154260509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939081-A-T

154260522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939094-G-A

154260522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939094-G-C

154260674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939135-T-C

154260675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939136-G-A

154260719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939161-T-C

154260734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939176-G-A

154260736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939178-G-T

154260762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939203-T-A

154260762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939203-T-C

154260783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939225-T-G

154260933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6939280-T-C

154265709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946329-A-G

154265742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946355-G-T

http://identifiers.org/hco/6/GRCh38#154265776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6946386-C-A

154265776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946386-C-G

154265778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946388-G-A

154265778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946388-G-T

154265815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946426-C-T

http://identifiers.org/hco/6/GRCh38#154265834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6946436-C-A

154265834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946436-C-T

154265847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946453-T-C

http://identifiers.org/hco/6/GRCh38#154265864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6946470-A-C

154265864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946470-A-T

http://identifiers.org/hco/6/GRCh38#154265874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6946480-C-A

154265885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946491-G-A

154265885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946491-G-C

154265885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946491-G-T

154265889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946495-G-A

154265889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946495-G-T

154265903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946509-G-A

154265968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6946580-G-A

154265968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6946580-G-T

154265999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946611-G-A

154265999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946611-G-C

154265999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946611-G-T

154266082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946694-A-T

154266098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946710-G-C

154266706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946958-A-T

154266739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6946985-G-T

154266939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6947175-G-A

154266939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6947175-G-C

154267041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6947762-T-C

154267098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6947815-A-G

154269202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6951918-T-G

154269285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952017-T-C

154269723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952478-C-G

154269742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952497-C-T

154269806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952550-G-A

154269889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952620-A-G

154269889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952620-A-T

154269896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952624-C-G

http://identifiers.org/hco/6/GRCh38#154269923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6952652-C-A

154269935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952664-G-A

154270000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952717-G-T

154270072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952766-T-A

154270074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952768-C-T

154270079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952775-G-A

154270101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952793-C-T

154270107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952799-G-A

154270158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952846-A-T

154270175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952863-T-C

154270175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6952863-T-G

154272172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6954955-T-C

154272177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6954960-T-C

154272207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6954986-C-T

154272217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6954996-G-A

154272444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6955224-T-C

154272462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6955242-T-C

154272628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6955415-A-G

154272672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6955455-A-G

154272720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6955510-G-A

154273102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6956251-A-G

154273140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6956289-C-T

http://identifiers.org/hco/6/GRCh38#154273403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6956553-C-A

154273410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6956560-G-A

http://identifiers.org/hco/6/GRCh38#154273428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6956574-C-A

154273457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6956602-G-A

154273457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6956602-G-C

154274103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6956891-A-T

http://identifiers.org/hco/6/GRCh38#154274249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6957009-A-C

154274468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6957227-C-T

154274553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6957312-C-T

154274620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6957385-C-T

154275022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6957674-T-C

154275096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6957731-A-G

http://identifiers.org/hco/6/GRCh38#154275119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6957752-A-C

154275137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6957770-A-T

154275470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6958058-C-T

154275515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6958100-G-C

154275521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6958106-C-T

154275644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6958235-A-G

154275720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6958311-G-A

http://identifiers.org/hco/6/GRCh38#154275734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6958321-C-A

154275734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6958321-C-G

154276690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959081-G-A

154276721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959109-G-A

154276752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959136-G-A

http://identifiers.org/hco/6/GRCh38#154276766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6959150-A-C

154276766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959150-A-T

154276822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959195-C-T

154276951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959280-C-T

154277194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959520-C-T

154277463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6959896-C-T

154277671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960544-G-A

http://identifiers.org/hco/6/GRCh38#154277715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6960590-C-A

http://identifiers.org/hco/6/GRCh38#154277727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6960602-C-A

154277727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960602-C-T

154277796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960668-C-T

154277891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960767-G-A

154277936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960816-T-C

154277953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960833-A-T

154278034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6960909-T-G

154285704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6969788-A-T

154285836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6969919-C-G

154285836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6969919-C-T

http://identifiers.org/hco/6/GRCh38#154286563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6970546-C-A

154286612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6970593-G-C

154286797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6970762-G-A

http://identifiers.org/hco/6/GRCh38#154287851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6971744-C-A

154287851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6971744-C-T

http://identifiers.org/hco/6/GRCh38#154287912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6971803-C-A

154288084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6972178-T-C

154288106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6972209-G-A

154288222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6972295-T-C

154288281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6972361-G-C

http://identifiers.org/hco/6/GRCh38#154289291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6972692-A-C

154289326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6972726-T-G

154289464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6972869-A-G

http://identifiers.org/hco/6/GRCh38#154289646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6973072-A-C

154289728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 5 prime UTR variant
orthologous variants: 6973157-T-A

154290866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6973821-G-A

154290866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6973821-G-T

154292442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6974595-A-G

154292597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6974746-G-A

http://identifiers.org/hco/6/GRCh38#154292944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#6975026-C-A

154293381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6975401-G-C

154293576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6975594-A-T

http://identifiers.org/hco/6/GRCh38#154293579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6975597-A-C

154293775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6975792-T-C

154293878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6975894-T-C

154293879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6975895-G-A

154293889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6975905-T-C

http://identifiers.org/hco/6/GRCh38#154294104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6976118-C-A

154294160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6976175-G-A

154294373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6976448-G-A

154295571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6977115-G-A

154295571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6977115-G-T

154296017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6977487-G-A

154296017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6977487-G-C

154296310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6977683-G-A

154297351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6978061-C-T

http://identifiers.org/hco/6/GRCh38#154297441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6978141-C-A

154297441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6978141-C-T

154297481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6978155-C-T

154297547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6978215-A-G

154297693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6978355-C-T

154298339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6979148-T-C

154298482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6979292-T-C

154298491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6979301-G-A

154299293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6979897-G-A

154302019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6984697-G-T

154302026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6984701-A-G

154302039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6984709-T-C

154302159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6984813-T-C

154302176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6984830-A-G

154302215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6984867-T-C

154302393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985033-C-G

154302632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985142-G-A

154302632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985142-G-C

154302661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985163-G-C

154303545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985564-T-C

154303549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985568-T-G

154303554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6985573-T-C

154308534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6986600-G-A

154308534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6986600-G-T

154308552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6986618-T-C

154308574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6986647-C-T

154317857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6989102-A-G

http://identifiers.org/hco/6/GRCh38#154317933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6989165-C-A

154318155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6989368-A-G

154318497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6989654-G-A

154318905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6989989-A-G

154318975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990052-C-T

154319112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990186-C-G

154319162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990237-C-T

154319314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990386-T-A

154319321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990393-G-A

154319350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990422-C-T

154319530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990610-C-T

http://identifiers.org/hco/6/GRCh38#154319706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6990787-C-A

154319706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990787-C-G

154319754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6990836-A-G

154320219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6991273-A-G

154320241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6991295-T-A

http://identifiers.org/hco/6/GRCh38#154320328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#6991384-C-A

154320400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6991457-A-T

154320432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6991480-G-A

154321236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992094-G-A

154321367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992212-G-A

154321415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992252-G-C

154321429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992263-C-T

154321432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992266-A-G

154321447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992281-C-G

154321504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992330-G-A

154321531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992352-A-T

154321854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992669-C-T

154321890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992707-C-T

154321928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992750-T-C

154322109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6992934-T-C

154322515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 6993216-C-T

154324960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7000059-G-A

154324960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7000059-G-T

154325060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7000155-G-A

154325060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7000155-G-C

154325072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7000167-A-T

154325208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7000304-T-C

154347712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004233-G-A

154347712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004233-G-T

154347909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004664-G-T

154347941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004696-T-C

154348034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004790-A-G

154348129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004886-C-T

154348137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7004894-C-T

154348264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7005005-G-A

154348314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7005056-G-A

154348345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7005087-T-A

154348482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7005224-C-T

http://identifiers.org/hco/6/GRCh38#154348883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7005606-A-C

154348961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7005667-T-C

154349625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7006148-A-G

154349666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7006190-C-T

154349699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7006220-G-T

154350036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7006973-G-A

154350085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7007021-C-G

154350325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7007551-A-G

154350434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7007658-T-C

154350536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7007756-C-T

154352699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7009614-G-A

154352723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7009638-G-A

154352850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7010325-G-T

154353042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron_variant, undefined
orthologous variants: 7010502-A-T

154353114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7010573-T-G

154353257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7010707-G-T

http://identifiers.org/hco/6/GRCh38#154353407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7010872-C-A

154353904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011272-T-A

154353904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011272-T-G

154353942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011314-T-C

154353954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011326-C-T

154354067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011440-C-T

154354287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011634-C-G

154354352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011686-G-C

154354364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011698-T-C

154354386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011720-C-T

154354387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011721-G-A

154354391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011725-C-T

http://identifiers.org/hco/6/GRCh38#154354415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7011749-A-C

154354415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011749-A-G

154354415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011749-A-T

http://identifiers.org/hco/6/GRCh38#154354471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#7011791-A-C

154354471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011791-A-T

154354562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011870-G-A

154354562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011870-G-C

154354562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011870-G-T

154354592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7011899-G-A

154354633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7012590-C-T

154354692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7012640-T-C

154354788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7012727-T-C

154354841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7012848-T-C

154355229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7013225-T-C

154355405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7013386-A-T

154355987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7013467-C-T

154356199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7013684-T-A

154356212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7013697-T-C

154356546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7014026-A-T

154356599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7014075-A-G

154356645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7014104-C-T

154356653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: intron variant
orthologous variants: 7014108-A-T

154356756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21204
most severe consequence: 5 prime UTR variant
orthologous variants: 7014214-T-G