16986036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140734564-G-A

16986075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140734527-G-A

16986228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140734380-A-G

16986237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140734371-G-C

16986439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140734175-G-A

16986502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140734118-A-G

16986659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733960-G-A

http://identifiers.org/hco/1/GRCh38#16986677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140733937-C-A

16986723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733888-C-T

http://identifiers.org/hco/1/GRCh38#16986726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140733885-C-A

16986726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733885-C-T

http://identifiers.org/hco/1/GRCh38#16986744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140733867-C-A

http://identifiers.org/hco/1/GRCh38#16986774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140733841-C-A

16986857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140733760-C-T

16986997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140733621-T-G

16987029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140733592-G-A

16987070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 140733551-T-C

16987151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733470-G-A

16987151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733470-G-C

16987184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733437-C-T

http://identifiers.org/hco/1/GRCh38#16987202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140733419-A-C

16987202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140733419-A-G

16987401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140733269-G-A

16987401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140733269-G-T

http://identifiers.org/hco/1/GRCh38#16987568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140733137-C-A

16987568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140733137-C-T

16987569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140733136-G-A

16987890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140732893-G-A

http://identifiers.org/hco/1/GRCh38#16988073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140732753-C-A

16988073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140732753-C-T

16988136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 140732673-A-G

16988211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140732598-G-A

16988217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140732592-A-G

16989501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731878-G-A

16989501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731878-G-T

http://identifiers.org/hco/1/GRCh38#16989648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140731789-A-C

16989648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731789-A-G

16989706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140731741-T-C

16989718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140731729-T-A

http://identifiers.org/hco/1/GRCh38#16989739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140731708-A-C

16989773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140731674-G-A

16989848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731628-G-C

16989900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140731582-T-C

16989955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140731527-T-C

16989966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140731516-T-G

16990093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731390-G-A

16990134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140731348-C-T

http://identifiers.org/hco/1/GRCh38#16990163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140731319-C-A

16990295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140731188-T-A

16990300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731183-G-A

16990300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731183-G-T

16990332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140731149-G-T

http://identifiers.org/hco/1/GRCh38#16991715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140730603-C-A

16991715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730603-C-G

16991715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730603-C-T

16991862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140730456-G-A

16991893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730425-C-T

16991902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730416-G-A

16991903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730415-G-C

16991952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730369-C-T

16991993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730338-C-G

16991993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730338-C-T

16992003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730334-G-C

16992012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140730325-G-A

http://identifiers.org/hco/1/GRCh38#16992028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140730309-C-A

16992036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140730301-C-T

16992169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730164-G-A

16992173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730160-C-G

16992178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730155-G-A

16992178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730155-G-T

16992179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730154-C-G

16992209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730124-C-G

16992217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140730118-G-A

16992404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 140729931-T-C

http://identifiers.org/hco/1/GRCh38#16992456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140729883-C-A

16992588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140729759-G-A

http://identifiers.org/hco/1/GRCh38#16992726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140729660-A-C

16992818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729583-T-C

16993608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729420-T-C

16993653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140729375-C-T

16993734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140729294-C-G

16993734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140729294-C-T

16993746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140729282-G-A

16993746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140729282-G-T

16993773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140729255-T-C

16993792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140729236-A-G

16993804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140729224-A-G

16993819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140729209-T-C

http://identifiers.org/hco/1/GRCh38#16993887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140729152-C-A

16993887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729152-C-T

16993889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729150-G-A

16993889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729150-G-T

16993893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729146-A-G

http://identifiers.org/hco/1/GRCh38#16993895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140729144-C-A

16993895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729144-C-T

16993959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140729099-A-G

http://identifiers.org/hco/1/GRCh38#16995751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140728358-C-A

http://identifiers.org/hco/1/GRCh38#16995752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140728357-C-A

16995753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728356-A-G

16995754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728355-G-A

16995754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728355-G-T

16995755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728354-T-C

http://identifiers.org/hco/1/GRCh38#16995773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140728340-C-A

16995773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728340-C-G

16995773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728340-C-T

16995871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728254-T-C

16995912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728234-G-A

16995912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728234-G-T

16996025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728133-G-C

16996082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140728076-A-G

16996258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140727894-T-G

16996272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140727880-G-A

16996272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140727880-G-C

http://identifiers.org/hco/1/GRCh38#16996337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140727813-C-A

16996337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140727813-C-T

http://identifiers.org/hco/1/GRCh38#16996352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140727797-C-A

16996368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140727781-G-A

16996368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140727781-G-C

16996390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140727758-G-A

16996454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140727694-T-C

http://identifiers.org/hco/1/GRCh38#16996533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140727601-A-C

16996951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140726655-G-A

16996951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140726655-G-T

16996992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140726614-C-T

16997046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140726566-T-G

16997366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140726299-C-T

16997514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140726169-G-T

http://identifiers.org/hco/1/GRCh38#16999931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140724185-A-C

http://identifiers.org/hco/1/GRCh38#17000006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140724113-C-A

17000006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140724113-C-T

17000055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140724064-G-A

http://identifiers.org/hco/1/GRCh38#17000199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140723940-C-A

17000199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723940-C-G

17000199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723940-C-T

http://identifiers.org/hco/1/GRCh38#17000200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140723939-C-A

17000200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723939-C-G

17000200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723939-C-T

17000216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723923-G-A

17000216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723923-G-C

17000216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723923-G-T

17000231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723913-G-A

17000231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723913-G-C

http://identifiers.org/hco/1/GRCh38#17000233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140723911-C-A

17000317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140723828-G-A

17000325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723818-G-A

17000333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723810-G-A

17000334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723809-G-A

17000334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723809-G-T

http://identifiers.org/hco/1/GRCh38#17000353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140723791-C-A

17000353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723791-C-T

17000494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140723651-G-A

17000494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140723651-G-C

17000671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 140723504-A-G

17001593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723275-C-G

17001600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723268-C-T

17001697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723160-A-T

17001706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723146-G-A

17001831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140723040-A-G

17001889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722992-G-A

17001889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722992-G-T

17001892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722989-G-A

17001892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722989-G-C

17001892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722989-G-T

17001917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722971-G-C

17001917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722971-G-T

http://identifiers.org/hco/1/GRCh38#17001943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140722961-C-A

17001966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722956-G-A

17001966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722956-G-T

http://identifiers.org/hco/1/GRCh38#17001971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140722951-C-A

17001971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722951-C-T

17002026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 140722944-A-G

17002080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140722890-A-G

17002218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722777-G-T

17002227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722768-G-T

17002235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722760-A-T

17002239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722756-G-A

17002239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722756-G-C

17002239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722756-G-T

17002279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722729-T-C

17002308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 140722700-T-C

17002358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 140722650-G-A

17002393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722619-G-A

17002393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722619-G-C

17002393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722619-G-T

17002472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722546-T-A

17002772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140722307-G-A

17003244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140721955-C-T

http://identifiers.org/hco/1/GRCh38#17004183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#140721832-C-A

17004183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 140721832-C-T

http://identifiers.org/hco/1/GRCh38#17004277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140721748-C-A

17004277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140721748-C-G

17004443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140721593-A-G

17004467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140721569-T-C

17004581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 140721492-T-C

17004671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140721404-A-G

17004674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 140721401-G-T

17005025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 140721152-G-A

17005048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 140721129-C-T

17005145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, undefined
orthologous variants: 140721032-G-A

17005145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, undefined
orthologous variants: 140721032-G-T

http://identifiers.org/hco/1/GRCh38#17005199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140719973-C-A

17005199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719973-C-G

17005199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719973-C-T

http://identifiers.org/hco/1/GRCh38#17005261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140719924-C-A

17005261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719924-C-T

17005279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719896-G-A

17005614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719587-G-C

17005660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719553-C-T

17005676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140719543-C-G

17005676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140719543-C-T

17005782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140719437-T-C

17005782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140719437-T-G

17005785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 140719434-A-G

17005813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140719404-G-A

17007195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140718987-C-T

17007196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140718986-C-T

http://identifiers.org/hco/1/GRCh38#17007542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140718558-A-C

17007551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140718549-T-C

http://identifiers.org/hco/1/GRCh38#17007650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140718457-C-A

17007674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140718434-C-T

http://identifiers.org/hco/1/GRCh38#17007699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140718407-C-A

17007781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140718291-G-A

17009792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140716537-G-A

http://identifiers.org/hco/1/GRCh38#17009921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#140716397-A-C

17010998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140714833-C-T

17011453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30213
most severe consequence: intron variant
orthologous variants: 140714474-C-T