105136318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45212198-G-A

http://identifiers.org/hco/6/GRCh38#105136320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45212196-C-A

105136320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45212196-C-T

http://identifiers.org/hco/6/GRCh38#105136334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45212182-C-A

105136334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45212182-C-T

105136380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45212143-G-T

105136410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 45212115-A-G

http://identifiers.org/hco/6/GRCh38#105137019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45211927-C-A

105137036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45211909-G-A

105137036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45211909-G-T

105137055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45211890-C-T

http://identifiers.org/hco/6/GRCh38#105137134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45211850-C-A

http://identifiers.org/hco/6/GRCh38#105137141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45211845-C-A

105137141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45211845-C-G

105137143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45211843-G-A

105137206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45211801-G-C

105137267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45211750-G-A

105137267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45211750-G-C

105137267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45211750-G-T

105138572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45210374-A-G

105138572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45210374-A-T

http://identifiers.org/hco/6/GRCh38#105138584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45210362-C-A

105145056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45207378-G-T

http://identifiers.org/hco/6/GRCh38#105145064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45207370-A-C

105145277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45207141-C-T

105145323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45207094-G-A

105145353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45207068-T-C

105145395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206988-C-G

105145408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206978-A-G

http://identifiers.org/hco/6/GRCh38#105145836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45206609-C-A

105145899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206590-A-G

105145980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206511-G-A

105145995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206499-C-T

105146168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206354-A-G

105146580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206141-G-A

105146746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45206089-T-A

105146945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45205929-G-A

105146952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45205922-A-G

105147028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45205779-G-A

105147138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45205679-G-T

105147144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45205673-A-G

105147301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: non coding transcript exon variant
orthologous variants: 45205507-C-G

105147415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45205398-A-G

105147499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45205364-G-C

105147499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45205364-G-T

105147580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45205331-T-C

105147621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45205297-A-G

105147931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45205048-G-T

105148089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45204903-G-A

105148094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45204898-T-C

105148116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45204876-T-A

105148133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45204858-C-G

105148317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45204674-C-T

105148774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45204250-T-A

105149241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201714-C-G

105149269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201649-A-G

105149374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201507-C-T

http://identifiers.org/hco/6/GRCh38#105149424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45201458-C-A

105149515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201373-A-G

105149611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201268-T-C

105149618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201262-A-G

105149659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201218-A-G

105149659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201218-A-T

105149688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45201190-A-G

105152702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45199244-T-A

105152707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45199239-C-T

105152858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45199093-A-G

105152867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45199084-G-A

105152867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45199084-G-C

http://identifiers.org/hco/6/GRCh38#105153053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45198934-A-C

105153334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45198688-C-T

105154057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45198184-G-A

105154341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45198051-G-A

105154343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45198049-A-T

http://identifiers.org/hco/6/GRCh38#105154430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45197974-C-A

105154430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197974-C-G

105154430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197974-C-T

105154610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45197835-G-C

105154610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 45197835-G-T

105154685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197766-G-C

105154716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197735-T-C

105154805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197651-C-T

105155001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197469-C-G

105155035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197422-T-C

105155409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197028-C-T

105155430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45197008-C-G

105155491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196949-C-G

105155491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196949-C-T

105155653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196884-T-A

105155721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196821-G-C

105155894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196641-G-C

105155914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196622-A-G

105155951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196590-T-C

105156460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196185-C-T

105156489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45196111-G-A

105156688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195627-G-T

105156699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195618-G-C

105156724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195594-C-T

105156755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195567-A-G

http://identifiers.org/hco/6/GRCh38#105156873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45195451-C-A

105156873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195451-C-G

105156873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195451-C-T

105156874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195450-G-A

105157066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195307-A-G

105157188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45195234-C-T

105157575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45194872-A-G

105157750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45194722-C-T

105158138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194346-G-A

105158138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194346-G-C

105158138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194346-G-T

http://identifiers.org/hco/6/GRCh38#105158157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45194327-A-C

105158157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194327-A-G

105158162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194322-T-C

105158162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194322-T-G

105158173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194311-G-A

105158173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194311-G-T

http://identifiers.org/hco/6/GRCh38#105158261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45194237-C-A

105158280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194218-T-A

105158288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194210-A-G

105158346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194150-G-A

105158346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194150-G-T

105158439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194108-T-C

105158443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194102-T-A

105158498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45194046-T-C

http://identifiers.org/hco/6/GRCh38#105158648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45193896-A-C

105158648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45193896-A-G

105158780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45193595-G-T

http://identifiers.org/hco/6/GRCh38#105158829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45193486-A-C

105159596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192764-T-C

105159638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192712-T-C

105159638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192712-T-G

http://identifiers.org/hco/6/GRCh38#105159646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45192704-C-A

105159646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192704-C-G

105159646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192704-C-T

http://identifiers.org/hco/6/GRCh38#105159665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45192681-C-A

105159665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192681-C-T

105159861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192483-G-A

105159861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192483-G-C

105159861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192483-G-T

105159901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192444-G-A

105159901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192444-G-T

http://identifiers.org/hco/6/GRCh38#105159965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45192380-C-A

105159965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192380-C-T

105159979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45192375-A-G

105160125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 45192236-T-A

http://identifiers.org/hco/6/GRCh38#105160173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45192179-C-A

105161093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191698-A-G

105161158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191639-T-C

105161161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191636-C-T

105161303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191485-T-G

105161308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191480-C-G

105161308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191480-C-T

105161349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45191439-G-T

http://identifiers.org/hco/6/GRCh38#105161398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45191399-A-C

105161518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45191280-A-G

105161569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45191229-G-A

105161839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45190959-T-C

105161949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45190853-G-T

105162094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45190721-A-G

105162094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45190721-A-T

105162153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45190662-G-A

105162153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45190662-G-T

105162204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45190610-G-T

http://identifiers.org/hco/6/GRCh38#105162259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45190553-C-A

105162259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45190553-C-T

105162267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45190545-T-G

http://identifiers.org/hco/6/GRCh38#105162268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45190544-A-C

105162373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45190444-T-G

105162645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45190046-T-C

http://identifiers.org/hco/6/GRCh38#105162731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45189988-A-C

105162731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45189988-A-G

105162760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45189959-T-G

http://identifiers.org/hco/6/GRCh38#105162807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45189921-A-C

105163013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45189712-G-C

105163279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45189137-G-A

105163325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45189091-C-T

105163331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45189085-A-T

105163741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45188737-A-G

105163822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45188634-T-C

http://identifiers.org/hco/6/GRCh38#105163875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45188583-C-A

http://identifiers.org/hco/6/GRCh38#105163876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45188582-C-A

105164283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45188188-G-A

105164684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187822-C-T

105164744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187763-T-A

105164974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187551-C-T

105165138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187353-G-A

105165468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187100-A-G

105165508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187071-T-C

105165588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187013-G-A

105165591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45187010-C-T

105166003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45186599-T-G

105173331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45176194-A-G

105173439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45176048-T-C

105173453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45176027-G-A

105173631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45175888-C-T

105173754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45175650-G-A

105173754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45175650-G-T

http://identifiers.org/hco/6/GRCh38#105173844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45175568-C-A

http://identifiers.org/hco/6/GRCh38#105173926-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45175503-A-C

105174013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45175412-C-T

105174015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45175410-C-T

105177019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45170459-G-A

105177019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45170459-G-C

105177019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45170459-G-T

105177075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45169734-C-T

105177100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45169714-C-T

105177105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45169709-C-T

105177131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45169683-A-G

105177367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45169488-A-G

105177764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45167709-C-T

105178016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45167238-T-C

105178516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166796-G-C

105178564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166748-A-G

105178630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166716-T-A

http://identifiers.org/hco/6/GRCh38#105178632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45166714-A-C

105178632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166714-A-G

105178632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166714-A-T

105178804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166552-C-G

105178913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166436-G-C

105178976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166395-T-G

http://identifiers.org/hco/6/GRCh38#105179073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45166260-C-A

105179080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166253-T-G

105179170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166160-T-A

105179170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166160-T-C

105179246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166078-G-A

105179275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45166062-C-T

105179378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45165983-A-G

105179505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45165871-T-C

http://identifiers.org/hco/6/GRCh38#105179569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45165827-C-A

105179569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45165827-C-T

105179595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45165813-G-A

http://identifiers.org/hco/6/GRCh38#105179630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45165790-C-A

http://identifiers.org/hco/6/GRCh38#105179702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45165757-C-A

http://identifiers.org/hco/6/GRCh38#105179742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45165736-C-A

105179742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165736-C-T

105179853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165655-C-G

105179853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165655-C-T

105179856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165652-A-G

105179873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165636-C-G

105179873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165636-C-T

105179881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165628-T-C

105179911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165591-G-A

105179932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165576-G-A

105179932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165576-G-T

http://identifiers.org/hco/6/GRCh38#105179949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45165559-C-A

105179949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165559-C-T

105179956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165552-C-G

105179968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 45165532-C-G

105180846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45164522-C-T

http://identifiers.org/hco/6/GRCh38#105182066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45162842-A-C

105182180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45162735-A-G

105182274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45162651-A-G

105182301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45162624-T-A

105182312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45162613-A-G

http://identifiers.org/hco/6/GRCh38#105182334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45162591-C-A

105182469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45162493-G-A

105182473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45162490-T-C

105188787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45153665-A-T

105188807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45153647-T-A

105188844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45153624-T-C

105188930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45153532-G-A

105189068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45153412-T-C

105189720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45152878-A-G

http://identifiers.org/hco/6/GRCh38#105190714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45151331-C-A

105190714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151331-C-T

105190787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151291-G-A

105190787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151291-G-T

105190886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151196-C-T

105190928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151153-G-A

105190937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151142-C-T

105190946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151133-T-C

105191047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45151034-G-A

105191344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45150746-A-G

105191392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45150698-C-T

105191472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45150598-T-C

105192888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45149822-A-G

105193768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45149380-A-G

105193911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45149254-G-A

105193952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45149213-C-T

http://identifiers.org/hco/6/GRCh38#105194037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45149128-A-C

105194545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45149004-G-T

105194695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45148855-G-C

105194710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45148840-G-A

105194710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45148840-G-C

105194710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45148840-G-T

105194768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45148784-G-A

105195131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21223
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45148436-C-T