10718156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 21336327-A-G

http://identifiers.org/hco/19/GRCh38#10718311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21336460-C-A

10718311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21336460-C-T

http://identifiers.org/hco/19/GRCh38#10718500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21336648-C-A

10718500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336648-C-T

10718606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336743-C-T

10718612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336765-G-A

10718612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336765-G-T

10718653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 21336793-T-A

10718653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 21336793-T-C

10718664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336804-G-A

10718664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336804-G-T

http://identifiers.org/hco/19/GRCh38#10718671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21336811-C-A

http://identifiers.org/hco/19/GRCh38#10718685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21336825-C-A

10718685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336825-C-G

10718685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21336825-C-T

10718779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21336943-T-C

http://identifiers.org/hco/19/GRCh38#10718878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21337040-C-A

10719065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21337193-G-A

10719683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21337605-A-G

10719683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21337605-A-T

10719698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21337621-T-C

10727657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21342021-A-T

10727667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21342031-G-T

10727767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21342113-C-G

10742148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359146-A-G

10742489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21359486-A-G

http://identifiers.org/hco/19/GRCh38#10747287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21362690-A-C

10747300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362703-A-G

10747448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362863-G-C

10747529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21362942-G-A

10747665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21363106-T-G

10752381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366217-C-T

10752388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366224-G-A

10752450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21366283-A-T

http://identifiers.org/hco/19/GRCh38#10759563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21368645-C-A

http://identifiers.org/hco/19/GRCh38#10759582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21368670-C-A

10759582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21368670-C-T

http://identifiers.org/hco/19/GRCh38#10759583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21368671-C-A

10762697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21370260-G-C

10766753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21373260-G-A

10767018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21373516-A-G

10768980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374142-T-C

10769010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374166-G-T

10769157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374296-C-T

10769242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374364-G-A

10769242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374364-G-T

10769262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374384-G-T

10769455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374537-G-A

10769524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374582-G-T

10769834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374821-C-T

10769848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21374839-C-T

10772148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376530-C-T

10772236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376608-T-C

10772236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376608-T-G

10772434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376835-G-A

10772434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376835-G-T

http://identifiers.org/hco/19/GRCh38#10772469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21376868-C-A

10772469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21376868-C-T

10772552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21376951-A-G

10772627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 21377026-C-T

10775596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378716-G-T

10775647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21378766-G-A

10775716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21378841-C-T

10775869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21378994-C-T

http://identifiers.org/hco/19/GRCh38#10775910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21379035-A-C

http://identifiers.org/hco/19/GRCh38#10777173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21382694-C-A

10777173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21382694-C-T

10782812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383762-T-C

10782844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383791-G-A

10782847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383797-G-A

10782847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383797-G-T

10782849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383799-G-A

10782851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383801-G-A

10782932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21383883-C-T

http://identifiers.org/hco/19/GRCh38#10783024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21383973-A-C

10783127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21384076-C-T

10783133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21384082-T-C

10786533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21385800-C-G

10786533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21385800-C-T

10786602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21385866-A-G

10786602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21385866-A-T

10793672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387723-A-G

10793687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387738-G-A

10793687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21387738-G-C

10793801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21387850-G-A

10793801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21387850-G-T

10793819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21387868-C-T

10793846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21387895-G-A

http://identifiers.org/hco/19/GRCh38#10793992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21388035-C-A

10795334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21389545-G-C

10795335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21389546-G-A

10795335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21389546-G-T

10795344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21389555-T-C

http://identifiers.org/hco/19/GRCh38#10795514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21389702-C-A

10795560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21389749-G-C

10795797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21389924-G-A

10795797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21389924-G-T

10795905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21390030-C-T

10795938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21390065-G-A

10795938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21390065-G-T

10796243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21390352-G-T

10797074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391187-G-A

10797100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391290-G-A

10797362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391683-G-A

10797362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391683-G-C

10797362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391683-G-T

10797562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391887-C-T

10797613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21391935-G-T

10797661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391972-G-A

10797661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21391972-G-T

10797693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21392002-A-T

10798082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392309-T-C

10798085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392312-C-T

10798109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392339-G-A

10798144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21392378-C-T

10800495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395355-A-G

10800519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395379-C-T

10800684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395539-G-A

10800684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395539-G-C

10800909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395769-G-T

10800930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21395795-C-T

10801230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396100-C-T

10801263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396153-G-A

10801263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396153-G-C

10801994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21396636-G-A

10802335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21396994-T-C

10803003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21397575-G-A

10803117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21397730-G-C

10803150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21397781-G-A

http://identifiers.org/hco/19/GRCh38#10803546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21398246-C-A

10803546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398246-C-G

10803546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398246-C-T

10803690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398394-C-T

http://identifiers.org/hco/19/GRCh38#10803717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21398421-C-A

10803717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398421-C-G

10803717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398421-C-T

10803726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398430-T-A

10803726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398430-T-C

10804027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398673-A-T

10804154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398781-C-G

10804238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398836-G-A

10804241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21398839-C-G

10805653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21400787-T-C

10805815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21400934-G-A

10805815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21400934-G-T

10806008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401129-C-T

http://identifiers.org/hco/19/GRCh38#10806032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21401152-A-C

10806109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401199-G-A

10806109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401199-G-T

10808253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401634-G-A

http://identifiers.org/hco/19/GRCh38#10808445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21401841-C-A

10808445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401841-C-G

10808445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401841-C-T

10808458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21401853-G-T

10808625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402008-G-C

10808726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402081-G-A

http://identifiers.org/hco/19/GRCh38#10808743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21402098-C-A

10808743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402098-C-G

10808743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402098-C-T

http://identifiers.org/hco/19/GRCh38#10808872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21402233-C-A

10808872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402233-C-T

http://identifiers.org/hco/19/GRCh38#10808873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21402234-A-C

10808873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402234-A-G

10808876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402237-G-A

10808876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402237-G-T

http://identifiers.org/hco/19/GRCh38#10808923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21402488-C-A

10808923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402488-C-T

10808963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402528-T-C

10808963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402528-T-G

http://identifiers.org/hco/19/GRCh38#10808968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21402533-C-A

10808968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402533-C-G

10808989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402554-G-T

10809015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402578-A-G

10809015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402578-A-T

10809063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402626-G-A

10809063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402626-G-T

10809149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21402710-C-T

10809196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21402833-G-T

http://identifiers.org/hco/19/GRCh38#10809230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21402875-C-A

http://identifiers.org/hco/19/GRCh38#10809457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21403061-C-A

10809457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403061-C-T

http://identifiers.org/hco/19/GRCh38#10809505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21403105-C-A

10809505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403105-C-T

http://identifiers.org/hco/19/GRCh38#10810129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21403581-C-A

10810129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403581-C-T

10810143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403595-G-A

10810143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403595-G-T

10810156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403610-A-G

10810166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403615-T-A

10810166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403615-T-C

10810276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21403735-C-T

http://identifiers.org/hco/19/GRCh38#10810608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21404054-C-A

10810608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404054-C-T

http://identifiers.org/hco/19/GRCh38#10810744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21404181-C-A

10810752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404189-T-C

http://identifiers.org/hco/19/GRCh38#10810775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21404206-C-A

10810775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404206-C-T

10810796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404227-T-C

http://identifiers.org/hco/19/GRCh38#10810837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21404337-C-A

10810837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404337-C-T

10810884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404395-T-G

10810891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404402-A-G

10811110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404554-G-T

10811406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404785-G-A

10811406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404785-G-C

10811406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404785-G-T

10811444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404830-G-A

http://identifiers.org/hco/19/GRCh38#10811445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21404831-C-A

10811445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404831-C-G

10811445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404831-C-T

10811545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404930-G-A

10811545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404930-G-T

10811569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21404956-C-T

10811739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405132-A-G

10811754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405149-C-T

10811845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405249-G-A

10811875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405289-C-T

http://identifiers.org/hco/19/GRCh38#10811892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21405344-C-A

10811993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405478-C-G

10812022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405563-A-G

10812022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405563-A-T

10812059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21405606-G-A

10812059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21405606-G-T

10812065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21405612-C-G

10812065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21405612-C-T

10812074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405622-T-C

10812074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405622-T-G

10812075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405623-G-A

10812075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405623-G-C

10812085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405637-G-A

10812085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405637-G-T

10812245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405781-G-A

10812249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405785-C-T

10812251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21405787-C-T

10816862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407316-T-C

10817036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407456-G-A

10817273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407675-C-T

http://identifiers.org/hco/19/GRCh38#10817311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21407708-C-A

10817399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407763-T-A

10817399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407763-T-C

10817430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21407795-A-G

10817456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21407821-T-C

10817507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407871-A-G

10817507-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407871-A-T

http://identifiers.org/hco/19/GRCh38#10817523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21407878-C-A

10817523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407878-C-T

10817528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21407883-A-G

10817643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21407980-G-A

10817643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21407980-G-T

10817728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408054-C-T

10817745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408070-G-T

10817764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21408083-T-G

http://identifiers.org/hco/19/GRCh38#10817836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#21408173-C-A

10817836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21408173-C-T

10817851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21408188-A-G

10817985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21408337-C-T

10819904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410501-G-A

10819904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410501-G-C

10819921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21410518-G-T

10823624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411419-T-C

http://identifiers.org/hco/19/GRCh38#10823635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21411430-C-A

10823635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411430-C-T

http://identifiers.org/hco/19/GRCh38#10823648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21411443-C-A

10823682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411477-G-T

10823729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411522-A-G

10823863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21411629-G-A

10823863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21411629-G-T

10823869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21411635-C-T

10823887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21411653-C-G

10823887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21411653-C-T

10823916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411681-C-G

10823916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411681-C-T

http://identifiers.org/hco/19/GRCh38#10823918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21411683-C-A

10823918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21411683-C-T

10825041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21414818-C-T

10825059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 21414840-A-G

10825087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21414868-A-T

10825104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21414885-C-G

10825104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21414885-C-T

10825284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21415055-C-T

10829134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21415824-G-A

10829158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21415848-T-C

10829158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21415848-T-G

10829230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21415920-T-C

10829230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21415920-T-G

10829251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21415941-G-A

10829251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 21415941-G-T

10829359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416043-G-A

10829359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416043-G-T

10829647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416363-G-C

10829692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416410-C-T

10829732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416461-G-A

http://identifiers.org/hco/19/GRCh38#10830037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21416686-C-A

10830040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416689-C-G

10830040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21416689-C-T

10830124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21416757-C-T

10830256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21416889-C-G

10830256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21416889-C-T

10830352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 21416985-C-G

http://identifiers.org/hco/19/GRCh38#10830431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21417057-C-A

10830438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21417064-T-C

10830543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21417164-G-A

10830773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21417395-G-C

10830824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21417444-C-G

http://identifiers.org/hco/19/GRCh38#10830846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21417474-C-A

http://identifiers.org/hco/19/GRCh38#10830895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21417557-C-A

10830954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21417607-C-T

10831080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21417730-C-T

http://identifiers.org/hco/19/GRCh38#10831101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21417753-C-A

10831182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21417833-G-C

10831251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21417872-A-G

10831251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21417872-A-T

10831377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21417993-T-C

10831377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21417993-T-G

http://identifiers.org/hco/19/GRCh38#10831587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21418150-C-A

10831587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21418150-C-T

10831658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21418230-T-C

10831768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21418307-G-A

10832001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21418519-A-G

10832501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21418914-G-A

10832501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21418914-G-T

10832620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419092-C-T

http://identifiers.org/hco/19/GRCh38#10832655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21419136-C-A

10832655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419136-C-T

http://identifiers.org/hco/19/GRCh38#10832673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21419168-C-A

10832673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419168-C-T

10832676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419171-T-C

http://identifiers.org/hco/19/GRCh38#10832748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21419249-C-A

10832748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419249-C-T

http://identifiers.org/hco/19/GRCh38#10832797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#21419297-C-A

10832797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419297-C-T

10832799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 21419299-C-G

10832992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 21419466-G-T

10833034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2974
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant, undefined
orthologous variants: 21419508-G-C