3039220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106651801-A-G

http://identifiers.org/hco/3/GRCh38#3039254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106651836-C-A

http://identifiers.org/hco/3/GRCh38#3039255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106651837-A-C

3039255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106651837-A-G

3039280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106651872-A-T

3039359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106651951-T-C

3039550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652134-A-G

3039603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652201-T-C

3039617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652216-T-A

3039617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652216-T-C

3039622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652221-G-C

3039732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652361-A-G

3039732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652361-A-T

3039757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652394-T-C

3039766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652403-T-A

3039766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652403-T-C

3039766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652403-T-G

3039801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652452-T-G

3039806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652457-G-A

3039806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652457-G-T

3039854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652502-G-A

3039854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652502-G-T

3039938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652587-G-A

3039938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106652587-G-C

3040141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 106652800-T-A

3040141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 106652800-T-C

3040141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 106652800-T-G

3040355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653002-G-A

3040355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653002-G-C

3040355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653002-G-T

3040388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 106653035-T-A

3040388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 106653035-T-G

3040389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 106653036-T-G

http://identifiers.org/hco/3/GRCh38#3040472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106653448-C-A

3040472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653448-C-T

3040491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653468-G-C

3040491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653468-G-T

http://identifiers.org/hco/3/GRCh38#3040509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106653490-C-A

http://identifiers.org/hco/3/GRCh38#3040562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106653591-C-A

3040562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653591-C-G

3040972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653711-T-C

3041012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653742-T-C

3041102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653828-T-G

3041130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653853-T-C

3041164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653887-G-T

3041195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106653918-A-G

3042054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655057-A-G

3042136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655147-C-T

3042154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655166-C-G

3042154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655166-C-T

3042212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655219-T-A

http://identifiers.org/hco/3/GRCh38#3042317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106655309-C-A

3042317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655309-C-G

3042380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655372-C-T

3042440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655432-G-A

3042471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655451-T-C

3042487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655467-T-A

3042487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655467-T-G

http://identifiers.org/hco/3/GRCh38#3042490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106655470-C-A

http://identifiers.org/hco/3/GRCh38#3042520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106655502-C-A

3042520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655502-C-G

3042557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655540-A-G

3042601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655590-T-C

3042688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655919-G-T

3042694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106655925-C-T

3042812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106656042-G-A

3042812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106656042-G-C

3042863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106656093-A-G

http://identifiers.org/hco/3/GRCh38#3042919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106656153-A-C

3042919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106656153-A-G

3043283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656521-T-G

http://identifiers.org/hco/3/GRCh38#3043306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106656544-C-A

3043306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656544-C-G

http://identifiers.org/hco/3/GRCh38#3043311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106656549-C-A

3043311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656549-C-T

3043331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656569-T-C

3043512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656750-G-A

3043512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106656750-G-C

http://identifiers.org/hco/3/GRCh38#3043536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106656774-C-A

3043762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106657004-C-G

3043762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106657004-C-T

3043872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106657122-A-G

3043913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658055-T-A

3043969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658121-T-C

3044008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658191-C-T

3044059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658284-G-A

3044090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658307-T-A

3044107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658324-T-C

3044367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106658662-G-T

3049428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106667182-T-A

3049444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106667198-G-A

3049484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106667220-C-G

3051243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106668873-C-T

3051392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669025-T-C

3051392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669025-T-G

http://identifiers.org/hco/3/GRCh38#3051683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106669329-C-A

3051683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669329-C-G

3051856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669502-G-T

3051961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669585-G-A

3051961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669585-G-T

3052040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669674-G-A

3052166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669776-C-T

3052292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106669895-G-A

3052728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670467-T-C

3052863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670614-C-G

3053375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670803-A-G

3053375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670803-A-T

3053441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670873-C-G

3053442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106670874-A-G

3053723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671135-C-T

3053729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671141-G-A

3053729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671141-G-T

3053753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671175-A-G

3053753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671175-A-T

3053787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671210-T-C

3053983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106671406-T-C

3053996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671415-C-T

3054013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671432-T-A

3054013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671432-T-C

http://identifiers.org/hco/3/GRCh38#3054095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106671510-A-C

3054095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671510-A-G

3054361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671941-C-G

3054373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106671953-A-T

3054491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106672074-A-G

3054596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106672172-T-A

3054761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106672319-G-C

3054768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106672326-G-A

3055506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673541-C-T

3055515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673550-G-C

3055515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673550-G-T

3055516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673551-C-T

3055668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673703-T-C

3055802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673831-A-T

3055884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673891-A-T

3055918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673923-C-T

3055982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673985-A-T

3055995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106673998-T-G

http://identifiers.org/hco/3/GRCh38#3056015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106674377-C-A

3056015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674377-C-T

3056067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674429-C-G

3056067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106674429-C-T

3056160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106674522-A-G

3056160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106674522-A-T

http://identifiers.org/hco/3/GRCh38#3056554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106674915-A-C

3056569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106674937-G-A

3056569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106674937-G-C

http://identifiers.org/hco/3/GRCh38#3056593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106674962-C-A

http://identifiers.org/hco/3/GRCh38#3056643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106675012-C-A

http://identifiers.org/hco/3/GRCh38#3056790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106675149-C-A

3056881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106675226-C-T

3057191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106675510-A-G

3057236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106675553-C-G

3057380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106675700-C-T

http://identifiers.org/hco/3/GRCh38#3057432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106675752-A-C

http://identifiers.org/hco/3/GRCh38#3057481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106675800-C-A

3057481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106675800-C-G

3057527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106675841-A-G

http://identifiers.org/hco/3/GRCh38#3057851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106676160-A-C

3057994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676304-C-T

http://identifiers.org/hco/3/GRCh38#3058065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106676375-C-A

3058065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676375-C-G

3058065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676375-C-T

3058223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676547-A-G

3058636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106676673-G-A

http://identifiers.org/hco/3/GRCh38#3059030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106677053-C-A

3059119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677142-T-C

3059123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677146-T-C

3059155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677180-G-A

3059155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677180-G-C

3059252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106677271-G-A

3059373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106677390-T-C

3059383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106677400-G-A

3059383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106677400-G-T

3059410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677427-T-C

http://identifiers.org/hco/3/GRCh38#3059472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106677488-A-C

3059472-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677488-A-T

3059526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677536-A-G

3059583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677593-G-C

3059845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106677853-G-C

3060151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678137-T-G

3060161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678147-T-G

3060398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678319-C-T

http://identifiers.org/hco/3/GRCh38#3060551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106678464-A-C

3060665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678593-G-A

3060681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678611-G-A

3060693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678623-G-C

3060752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678698-C-G

3060879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678776-T-C

3060938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678813-G-A

3060954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678829-G-T

3060964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678839-G-A

3060964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678839-G-T

3061005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678862-G-T

3061006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678863-C-T

3061044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678895-T-C

3061133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: non coding transcript exon variant
orthologous variants: 106678935-G-A

3061133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: non coding transcript exon variant
orthologous variants: 106678935-G-T

3061239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678982-T-C

http://identifiers.org/hco/3/GRCh38#3061240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106678983-C-A

3061240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106678983-C-T

3061271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106679014-G-T

http://identifiers.org/hco/3/GRCh38#3061346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106679090-C-A

3061469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106679218-T-C

3062318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106680826-A-G

3062537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681029-A-G

3062643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681126-C-T

3062740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681226-G-A

3062945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681666-G-T

3062973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681686-T-G

3063042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681752-G-A

3063042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681752-G-C

3063155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681866-C-T

3063234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681937-C-G

3063234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681937-C-T

3063279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106681969-G-A

http://identifiers.org/hco/3/GRCh38#3063334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106682016-C-A

http://identifiers.org/hco/3/GRCh38#3063762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106682154-A-C

3063875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682262-G-A

3063886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682270-A-G

3063926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682297-A-G

3063951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682317-G-A

3064194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682536-C-T

3064716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682814-A-G

3064923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682942-G-A

3064923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106682942-G-T

3065219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683704-T-C

3065219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683704-T-G

3065783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106683900-A-G

http://identifiers.org/hco/3/GRCh38#3065847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106683979-A-C

3065902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684039-A-T

3066031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684117-G-A

3066102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684187-G-A

http://identifiers.org/hco/3/GRCh38#3066220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106684303-C-A

3066220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684303-C-T

http://identifiers.org/hco/3/GRCh38#3066224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#106684307-C-A

3066224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684307-C-T

3066225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684308-T-A

3066225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684308-T-C

3066308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106684368-T-C

http://identifiers.org/hco/3/GRCh38#3066389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106684446-C-A

3066389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684446-C-G

3066483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684535-T-G

3066654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684719-C-T

3066714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684779-A-G

http://identifiers.org/hco/3/GRCh38#3066775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106684840-C-A

3066775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684840-C-G

3066775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684840-C-T

http://identifiers.org/hco/3/GRCh38#3066788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106684853-C-A

http://identifiers.org/hco/3/GRCh38#3066818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106684882-C-A

3066873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106684936-A-G

3066944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106685006-T-C

3066944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106685006-T-G

3066969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106685031-G-T

http://identifiers.org/hco/3/GRCh38#3066978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106685040-C-A

3066978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106685040-C-T

3068728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686910-C-G

http://identifiers.org/hco/3/GRCh38#3068740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106686923-C-A

3068740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686923-C-G

3068760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686943-G-A

3068760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686943-G-T

http://identifiers.org/hco/3/GRCh38#3068800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106686966-C-A

3068800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686966-C-G

3068800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686966-C-T

http://identifiers.org/hco/3/GRCh38#3068811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#106686977-C-A

3068811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106686977-C-T

3068949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106687178-G-T

3069083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106687778-G-A

3069083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106687778-G-C

3069083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39985
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106687778-G-T