http://identifiers.org/hco/7/GRCh38#35080308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24468598-A-C

35081227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24468984-T-C

http://identifiers.org/hco/7/GRCh38#35081243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24468999-C-A

35081264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469020-G-T

http://identifiers.org/hco/7/GRCh38#35081284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469040-C-A

35081284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469040-C-T

35081292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469048-T-G

35081399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469139-T-C

35081405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469144-G-T

http://identifiers.org/hco/7/GRCh38#35081410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469149-A-C

35081410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469149-A-G

35081580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469323-A-T

35081581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469324-G-T

http://identifiers.org/hco/7/GRCh38#35081671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469414-A-C

35081671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469414-A-G

35081692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469435-A-G

35081698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469441-A-G

http://identifiers.org/hco/7/GRCh38#35081794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469528-A-C

35081798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469532-T-C

http://identifiers.org/hco/7/GRCh38#35081872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469609-C-A

http://identifiers.org/hco/7/GRCh38#35081879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469619-C-A

35081879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469619-C-T

35082011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469724-A-G

35082056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469764-C-G

http://identifiers.org/hco/7/GRCh38#35082218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469931-A-C

35082221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469934-G-A

35082447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24470093-C-T

35082509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24470145-C-G

35082509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24470145-C-T

35088979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491031-T-G

35089209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491275-T-C

35089240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491311-T-C

35089274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491346-T-G

35089948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24491991-T-A

35090114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492128-A-G

http://identifiers.org/hco/7/GRCh38#35090291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24492397-A-C

35090291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492397-A-G

35090306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492412-G-T

35090388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492494-T-C

35090415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492521-A-G

35090592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492680-G-A

35090592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492680-G-T

35090683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492755-T-C

35090683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492755-T-G

35090733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492798-T-C

35090862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492936-A-G

35090862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492936-A-T

35090888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492960-C-T

35091060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493095-A-T

35091128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493225-T-C

http://identifiers.org/hco/7/GRCh38#35091254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493433-C-A

35091254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493433-C-T

http://identifiers.org/hco/7/GRCh38#35091315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493487-C-A

http://identifiers.org/hco/7/GRCh38#35091366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493536-C-A

35091492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493661-G-A

35091492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493661-G-C

35091498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493668-G-C

35091498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493668-G-T

http://identifiers.org/hco/7/GRCh38#35091536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493713-C-A

35091690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493913-T-C

35091690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493913-T-G

http://identifiers.org/hco/7/GRCh38#35091721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24493955-C-A

35091721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493955-C-T

35091754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493983-T-G

35091761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-A

35091761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-T

http://identifiers.org/hco/7/GRCh38#35091785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24494019-C-A

35091785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494019-C-T

35091939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494176-G-A

35091939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494176-G-C

http://identifiers.org/hco/7/GRCh38#35092056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24494298-A-C

35102861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24495727-C-G

35102861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24495727-C-T

35102978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24495833-T-C

35103182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496036-G-A

35103182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496036-G-T

http://identifiers.org/hco/7/GRCh38#35103272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24496117-C-A

35103272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496117-C-T

35103285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496130-G-A

35103285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496130-G-T

35104334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496516-A-T

35104496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496664-A-G

http://identifiers.org/hco/7/GRCh38#35104576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24496738-C-A

35104779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496938-T-G

35104830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496983-T-C

35104916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24497082-C-T

http://identifiers.org/hco/7/GRCh38#35105065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24497222-A-C

35105510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24497725-T-C

35105817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498040-T-C

http://identifiers.org/hco/7/GRCh38#35105962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24498261-C-A

35105962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498261-C-T

35106102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24498394-A-G

http://identifiers.org/hco/7/GRCh38#35106131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24498423-A-C

35106131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24498423-A-T

http://identifiers.org/hco/7/GRCh38#35106175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24498467-C-A

35106311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24498564-T-C

http://identifiers.org/hco/7/GRCh38#35106452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24498678-A-C

35106461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24498687-A-G

35106474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24498699-T-C

35106508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24498732-T-C

35114824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24527847-G-A

35115376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528264-C-T

35115459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528353-T-C

http://identifiers.org/hco/7/GRCh38#35117471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24528422-C-A

35117483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528442-G-T

35117517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528479-A-G

35117826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528814-G-C

35117826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528814-G-T

35117892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528872-G-A

35117892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528872-G-T

35118010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529063-T-C

35118197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529156-T-G

35118593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529425-C-T

35118908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529737-T-C

35118918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529747-G-T

35118949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529770-T-C

35119006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529820-T-C

35119043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529859-G-A

35119535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530287-A-G

35119575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530327-G-T

35119599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530356-A-G

35119850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530586-A-G

35119859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530595-A-G

35120472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538677-A-T

35120499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538703-G-A

http://identifiers.org/hco/7/GRCh38#35121286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24539212-C-A

35121286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539212-C-T

35121531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539470-G-A

35121531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539470-G-T

35121664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539595-G-T

35121698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539634-G-C

35121698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539634-G-T

35121766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539701-A-G

35122194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541276-C-T

35123118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541829-C-T

35123143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541858-A-G

35123156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541869-A-T

35124001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24542498-G-T

35124149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542626-T-C

35124270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542757-A-G

http://identifiers.org/hco/7/GRCh38#35124279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24542765-C-A

35132319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24555017-G-A

35132319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24555017-G-T

35132454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555121-T-A

35132454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555121-T-C

http://identifiers.org/hco/7/GRCh38#35132467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24555134-C-A

35132586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555252-C-G

35141114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24556439-T-A

35141114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24556439-T-C

35141149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556473-G-T

35141247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556829-A-G

35141586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557123-C-T

http://identifiers.org/hco/7/GRCh38#35141786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24557510-C-A

35141786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557510-C-T

35141837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557557-G-A

35141837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557557-G-T

35141978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557697-G-A

35141978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557697-G-T

http://identifiers.org/hco/7/GRCh38#35142026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24557747-C-A

35142227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557952-G-C

35142228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557953-C-G

35142271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557995-T-C

35142415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558144-C-T

35143677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569253-T-A

35143704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569267-G-T

35143756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569325-T-C

35145200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570068-T-C

35145390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570270-G-A

35145413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570293-C-T

35146005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570552-G-A

35146128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570644-G-A

35146128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570644-G-C

35146372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570877-T-C

35147106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571412-G-A

35147108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571414-A-G

35147109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571460-T-C

35147754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571985-A-G

35147810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24572040-T-C

35147952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572185-G-T

35148207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572418-G-A

35148266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572464-T-C

35148778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573047-G-A

35148779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573048-G-A

35148999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573126-T-G

35149484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573416-C-T

35149524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573449-G-C

35149561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573485-G-A

35149561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573485-G-C

35149701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573868-A-G

35149725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573906-T-C

35149819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574048-A-G

35149911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574121-G-C

35149941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574148-T-G

http://identifiers.org/hco/7/GRCh38#35149960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574167-C-A

http://identifiers.org/hco/7/GRCh38#35149979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574186-C-A

35149979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574186-C-T

35150023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574223-G-A

35150023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574223-G-T

35150042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574244-T-A

35150042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574244-T-C

35150046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574248-T-C

35150073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574275-A-G

35150073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574275-A-T

http://identifiers.org/hco/7/GRCh38#35150087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574289-C-A

http://identifiers.org/hco/7/GRCh38#35150106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574308-A-C

35150106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24574308-A-G

35150150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24574346-T-G

35150229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24574423-G-A

35150229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24574423-G-C

35150296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574484-A-G

35150297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574485-G-A

35150297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574485-G-T

http://identifiers.org/hco/7/GRCh38#35150347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574532-C-A

35150441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574648-T-A

35150455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574662-A-T

35150470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574677-T-A

35150470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574677-T-C

35161177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24577617-T-C

35161217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577653-A-G

35161224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577661-T-C

35161256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24577693-G-A

http://identifiers.org/hco/7/GRCh38#35161282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24577728-A-C

35161322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577763-C-T

35161846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578075-A-G

35161846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578075-A-T

http://identifiers.org/hco/7/GRCh38#35161924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24578146-C-A

35161924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578146-C-T

35162084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24578288-A-G

35162260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578444-G-A

35162485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578602-G-A

35162659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578768-T-C

35162683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578809-G-A

35162684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578810-T-C

35162962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579031-C-T

35163108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579140-C-G

http://identifiers.org/hco/7/GRCh38#35163164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24579192-A-C

35163164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579192-A-G

35163275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579257-C-T

35163353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579308-C-T

35163515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579507-C-G

35163520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579512-A-T

35163576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579538-A-G

35163630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579547-T-C

35163635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579552-T-C

http://identifiers.org/hco/7/GRCh38#35163827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24579704-C-A

35163987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579871-T-G

35164086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579980-T-C

35164383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580209-C-G

35164624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580395-G-A

35164663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580438-A-G

35164733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580477-T-C

35164783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580527-A-G

35164783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580527-A-T

35164805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580552-G-A

35164805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580552-G-C

35164805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580552-G-T

35164808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580555-T-C

35164809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580556-A-G

35164809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580556-A-T

http://identifiers.org/hco/7/GRCh38#35164810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580557-C-A

35164810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580557-C-G

35164810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580557-C-T

http://identifiers.org/hco/7/GRCh38#35164817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580564-C-A

35164817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580564-C-T

http://identifiers.org/hco/7/GRCh38#35164977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580723-C-A

35178674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591684-T-C

35178674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591684-T-G

35178767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591755-C-T

http://identifiers.org/hco/7/GRCh38#35178801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24591789-A-C

35178929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591890-C-T

35179123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24592074-A-G

35179153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24592104-T-A

35179153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24592104-T-C

35179153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24592104-T-G

35179190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592134-G-A

35179190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592134-G-T

http://identifiers.org/hco/7/GRCh38#35179280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24592231-C-A

http://identifiers.org/hco/7/GRCh38#35179366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24592289-C-A

35179406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592319-G-A

35179427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592340-A-G

35179620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592517-C-T

http://identifiers.org/hco/7/GRCh38#35180090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24593137-A-C

http://identifiers.org/hco/7/GRCh38#35180111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24593158-C-A

35180179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593225-T-C

35181369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601308-G-A

35181369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601308-G-C

35181369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601308-G-T

35181563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601499-A-G

http://identifiers.org/hco/7/GRCh38#35181566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601502-C-A

35181566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601502-C-G

35181566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601502-C-T

http://identifiers.org/hco/7/GRCh38#35181577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601513-C-A

35181577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601513-C-T

35182041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601876-T-A

http://identifiers.org/hco/7/GRCh38#35182144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601976-A-C

35182187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602019-G-T

http://identifiers.org/hco/7/GRCh38#35182305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24602132-C-A

35182440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602253-C-T

http://identifiers.org/hco/7/GRCh38#35182449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24602261-A-C

35182449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602261-A-G

35183008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602869-C-T

35183164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602972-T-A

http://identifiers.org/hco/7/GRCh38#35183236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603021-C-A

35183391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603139-A-T

35183664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603406-T-C

35184043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603788-A-G

35184044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603789-G-A

35184540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604250-T-C

35184906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604645-T-C

35185811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607169-G-A

35185811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607169-G-C

35185877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607238-G-A

35185877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607238-G-T

http://identifiers.org/hco/7/GRCh38#35185886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607247-C-A

35185886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607247-C-G

35185886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607247-C-T

35185901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607262-G-C

35185901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607262-G-T

35185904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607265-G-A

35185904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607265-G-T

35185924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607285-C-T

http://identifiers.org/hco/7/GRCh38#35185949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607320-C-A

35185949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607320-C-T

35186006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607406-T-A

35186006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607406-T-C

35186013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607418-G-A

35186013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607418-G-T

http://identifiers.org/hco/7/GRCh38#35186046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607472-C-A

35186051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607486-T-A

35186051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607486-T-C

35186053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607488-G-C

35186106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22305
most severe consequence: non coding transcript exon variant
orthologous variants: 24607528-G-T