9644828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67813631-G-A

9644828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67813631-G-T

http://identifiers.org/hco/17/GRCh38#9645204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67813316-C-A

9645204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67813316-C-T

9645435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67813061-T-A

9645435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67813061-T-C

http://identifiers.org/hco/17/GRCh38#9645479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67813033-C-A

9645479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67813033-C-T

9645571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812935-G-A

9645571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812935-G-T

http://identifiers.org/hco/17/GRCh38#9645577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67812929-C-A

9645577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812929-C-T

9645608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812897-G-A

9645608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812897-G-C

9645608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812897-G-T

9645649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812856-G-A

9645649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812856-G-T

9645727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812778-T-A

9645727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812778-T-C

9645727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812778-T-G

http://identifiers.org/hco/17/GRCh38#9645733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67812772-C-A

9645733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812772-C-G

9645733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812772-C-T

http://identifiers.org/hco/17/GRCh38#9645776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67812729-C-A

9645776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67812729-C-G

9645776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67812729-C-T

9645834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812665-G-A

9645834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812665-G-C

9645834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812665-G-T

9645849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812650-G-A

9645849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812650-G-C

9645849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812650-G-T

9645862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67812637-A-G

9645915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812590-G-A

9645915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812590-G-T

9646028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67812477-G-A

9646028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67812477-G-C

9646144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67812361-G-A

9646144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67812361-G-C

9646144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67812361-G-T

http://identifiers.org/hco/17/GRCh38#9646160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67812342-C-A

9646160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67812342-C-T

http://identifiers.org/hco/17/GRCh38#9646162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67812340-C-A

9646162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812340-C-T

http://identifiers.org/hco/17/GRCh38#9646163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67812339-C-A

9646163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67812339-C-T

9646379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67812102-A-G

9646485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67812015-G-A

9646730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67811821-G-A

http://identifiers.org/hco/17/GRCh38#9646935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67811627-C-A

9646949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67811613-G-T

9647048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67811544-G-A

9647067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67811525-A-G

9647183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67811455-T-C

9647196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67811442-T-C

9647282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67811354-C-G

9648186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67810524-G-A

9648343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67810362-A-G

9648374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 67810333-A-G

9648485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 67810188-G-A

http://identifiers.org/hco/17/GRCh38#9648492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67810181-A-C

9653245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67806155-A-G

9653819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67805687-C-T

9653914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67805594-C-T

9655954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67805277-G-A

9656084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67805153-C-T

9656276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67804853-T-A

9656284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67804822-T-G

9656564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67804550-C-G

9656593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67804526-G-T

9656648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67804491-T-A

9656651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67804488-G-A

9658654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802363-A-G

9658821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67802196-T-C

9659494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67801413-G-A

9659586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67801113-T-A

9660723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799969-A-G

9660847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799876-G-A

9660847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799876-G-T

9661153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799578-T-C

9661288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67799446-A-G

http://identifiers.org/hco/17/GRCh38#9661554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67799338-C-A

9662046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67798830-T-A

9666373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67795527-G-A

9666392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67795508-G-A

9666393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67795507-A-G

9666564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67795336-A-G

9666760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67795136-G-C

http://identifiers.org/hco/17/GRCh38#9666853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67795050-C-A

9666972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794941-C-T

9666988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67794927-G-A

9668055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793246-T-G

http://identifiers.org/hco/17/GRCh38#9668206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67793093-C-A

9668206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793093-C-G

9668296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67793010-C-T

http://identifiers.org/hco/17/GRCh38#9668455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67792877-A-C

9668626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67792717-G-A

9670699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791903-G-A

9670886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791725-T-G

9670994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791610-G-A

9670994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791610-G-T

9671018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791592-T-A

9671062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67791548-A-G

9674826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67789867-T-C

9674916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67789775-C-T

http://identifiers.org/hco/17/GRCh38#9674928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67789763-A-C

9674928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67789763-A-G

9674998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789684-C-T

http://identifiers.org/hco/17/GRCh38#9675132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67789569-A-C

9675132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789569-A-G

9675158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789544-G-C

9675249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789443-C-T

9675322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789381-C-T

9675330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789373-C-T

9675437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67789149-A-G

9675587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67788997-A-G

9675588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67788996-T-C

9675843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67788770-G-A

http://identifiers.org/hco/17/GRCh38#9675879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67788744-C-A

9675908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 67788724-C-T

9676498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67788315-T-C

9676804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67788122-C-T

9677183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 67787771-T-C

9679546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784829-G-T

9679563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784812-T-A

9679695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784659-G-A

9679960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784450-G-A

9679987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784423-C-T

9680063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784353-A-T

9680099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67784324-A-G

http://identifiers.org/hco/17/GRCh38#9680456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67783687-C-A

9680479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783664-A-G

9680703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783485-G-A

9680732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783456-A-G

9680772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783416-A-G

9680924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67783307-T-C

9681891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782786-G-C

9681891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782786-G-T

9681947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782730-G-T

http://identifiers.org/hco/17/GRCh38#9681956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67782721-A-C

http://identifiers.org/hco/17/GRCh38#9681964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67782713-A-C

9681964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782713-A-G

9682078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782591-G-T

9682222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782505-T-C

http://identifiers.org/hco/17/GRCh38#9682349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67782477-C-A

9682393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782466-C-T

http://identifiers.org/hco/17/GRCh38#9682604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67782435-A-C

9682701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782361-G-T

9682712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782350-T-C

9682712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782350-T-G

9682714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782348-G-T

9682962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782170-T-C

9682992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67782140-T-A

9683105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67781792-A-G

9683236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67781659-G-A

9683382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67781342-G-A

9683435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67780844-A-G

9685096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67779213-A-G

9685165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67779148-A-T

9685317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67779042-T-C

9686705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778773-G-T

9686719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778755-G-A

9686724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778750-A-G

9686725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778749-A-G

9686916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67778564-G-T

9686928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778552-T-A

9686928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778552-T-C

9686929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778551-G-A

9686929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778551-G-C

9686929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778551-G-T

9686941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778539-G-A

9686941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778539-G-T

9686971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778509-G-C

9686971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778509-G-T

9687278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778333-G-T

9687345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67778270-A-T

9687388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777836-G-A

9687446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777804-A-T

9687537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777715-A-G

9687578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777684-T-C

9687594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777679-C-T

9687602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777671-A-G

9687602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777671-A-T

9687605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777668-T-C

9687911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67777391-A-G

http://identifiers.org/hco/17/GRCh38#9687969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67777332-A-C

9689281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776704-G-A

9689283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776702-A-G

9690060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67776027-C-G

http://identifiers.org/hco/17/GRCh38#9690165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67775936-C-A

9690183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775919-C-T

http://identifiers.org/hco/17/GRCh38#9690258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67775836-A-C

9690293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775793-C-T

http://identifiers.org/hco/17/GRCh38#9690399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67775688-C-A

9690518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67775595-C-T

9692535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774657-G-A

http://identifiers.org/hco/17/GRCh38#9692571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67774631-C-A

9692571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774631-C-T

9692671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774578-G-A

9692740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774518-G-A

9692750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774507-G-A

http://identifiers.org/hco/17/GRCh38#9692854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67774402-A-C

9693050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774206-G-A

9693093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774170-A-T

9693119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67774141-C-T

http://identifiers.org/hco/17/GRCh38#9693122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67774138-C-A

9693122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67774138-C-G

9693122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 67774138-C-T

9693130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67774130-C-G

9693130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67774130-C-T

9693198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67774062-C-G

9693235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67774025-G-C

9693343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773932-C-G

http://identifiers.org/hco/17/GRCh38#9693346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67773930-A-C

9693351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773925-T-C

9693351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773925-T-G

9694300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773367-G-C

9694339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773346-G-A

9694393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67773283-C-G

9699754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772811-C-T

9699871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772379-A-G

9699938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772316-C-T

9700103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772173-G-T

9700105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772171-T-C

9700146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772133-G-T

9700148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772131-T-C

9700230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67772049-G-A

9700230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67772049-G-T

http://identifiers.org/hco/17/GRCh38#9700270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67772010-C-A

9700270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772010-C-G

9700274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772006-T-A

9700274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67772006-T-C

9700310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771967-T-G

http://identifiers.org/hco/17/GRCh38#9700323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67771952-C-A

9700325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771950-T-C

9700337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771938-G-A

9700337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771938-G-T

9700395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771881-G-A

9700395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771881-G-T

9700521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771792-C-T

9700593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771722-C-T

http://identifiers.org/hco/17/GRCh38#9700723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67771639-C-A

9700723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771639-C-T

9700733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771629-C-T

9700813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771551-A-T

http://identifiers.org/hco/17/GRCh38#9700990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67771390-C-A

9700990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771390-C-T

9701019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771368-G-T

9701026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771361-G-A

9701026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771361-G-T

9701053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771325-A-G

9701053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771325-A-T

9701060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771318-G-A

9701060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771318-G-T

9701066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771312-A-G

9701070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771308-G-T

9701074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771304-G-A

9701074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771304-G-T

9701080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771298-A-G

9701084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67771294-A-G

9701251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771071-G-A

9701251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771071-G-C

9701251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771071-G-T

http://identifiers.org/hco/17/GRCh38#9701263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67771063-C-A

9701263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771063-C-T

http://identifiers.org/hco/17/GRCh38#9701264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67771062-A-C

9701264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67771062-A-G

9701264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 67771062-A-T

9701280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771040-G-A

9701280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771040-G-C

9701280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771040-G-T

9701292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 67771028-C-T

http://identifiers.org/hco/17/GRCh38#9701451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67770869-C-A

9701451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67770869-C-T

http://identifiers.org/hco/17/GRCh38#9701604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67770716-C-A

9701604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67770716-C-T

9701622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67770698-A-T

9701643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67770677-T-C

http://identifiers.org/hco/17/GRCh38#9701832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67770471-C-A

9701832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67770471-C-T

9702598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67770188-C-T

9702635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67770154-T-A

9702828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67769975-A-T

9702880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67769942-G-A

http://identifiers.org/hco/17/GRCh38#9702886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67769936-C-A

9702930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67769896-G-T

9703144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67769703-A-G

http://identifiers.org/hco/17/GRCh38#9709821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67767482-C-A

9709852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67767455-T-C

http://identifiers.org/hco/17/GRCh38#9710018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67767293-C-A

http://identifiers.org/hco/17/GRCh38#9710057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67767254-C-A

9710057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67767254-C-T

9710145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67767150-G-A

9710145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67767150-G-C

9710145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67767150-G-T

9711030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766900-G-C

http://identifiers.org/hco/17/GRCh38#9711270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67766613-C-A

9711831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766415-T-G

9711854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766392-T-A

9711854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766392-T-C

http://identifiers.org/hco/17/GRCh38#9711907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67766315-C-A

9711907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766315-C-T

9711949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766269-C-G

9711949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766269-C-T

9712073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67766146-C-T

9712154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766071-G-A

9712154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766071-G-C

9712154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766071-G-T

9712166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766059-T-C

9712167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766058-T-A

9712167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766058-T-C

9712167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766058-T-G

9712184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67766047-G-T

9712252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765988-G-A

9712252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765988-G-C

9712252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67765988-G-T

9716560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756264-C-T

9716681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756149-G-T

9716751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756079-A-G

9716787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756031-G-A

http://identifiers.org/hco/17/GRCh38#9716795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67756024-C-A

9716795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67756024-C-G

http://identifiers.org/hco/17/GRCh38#9719263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67754728-C-A

9719345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67754646-A-G

9719681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67754441-G-A

9722558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752806-G-T

9722608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752766-T-C

9722880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752489-A-G

9722984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752386-C-T

9723226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67752144-T-G

9723510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751898-C-T

http://identifiers.org/hco/17/GRCh38#9723981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67751548-C-A

9724022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751507-T-G

9724095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751438-G-C

9724151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67751369-A-T

9724875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750439-G-A

9724899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750415-T-G

9724913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750401-A-G

9724975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750362-C-T

9725058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67750278-C-T

9725463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749759-A-G

9725883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749367-G-T

9725953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67749301-C-G

9726268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748983-G-A

9726268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748983-G-T

9726355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748927-G-A

9726414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748870-C-T

http://identifiers.org/hco/17/GRCh38#9727406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67748330-C-A

9727435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748280-T-C

9727582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67748039-A-G

9727652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747972-A-G

http://identifiers.org/hco/17/GRCh38#9727832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67747485-C-A

9727832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747485-C-G

http://identifiers.org/hco/17/GRCh38#9727941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67747381-C-A

9727941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 67747381-C-T

9727965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67747357-C-G

9727965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67747357-C-T

9727990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67747332-A-G

9728226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67747096-G-A

9728226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67747096-G-T

9728258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67747064-G-A

http://identifiers.org/hco/17/GRCh38#9728364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67746955-A-C

9728452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67746867-C-T

9728473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67746846-C-T

9728558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67746761-C-T

9728561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67746758-T-G

9728710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67746570-G-A

9728792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 67746503-G-A

9728806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67746489-T-C

9728973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 67746322-C-T

9729016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67746278-C-T

9729088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67746205-G-A

9729088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67746205-G-C

9729088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 67746205-G-T

http://identifiers.org/hco/17/GRCh38#9729095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#67746198-A-C

9729138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3 prime UTR variant
orthologous variants: 67746159-C-G

9729138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3 prime UTR variant
orthologous variants: 67746159-C-T

http://identifiers.org/hco/17/GRCh38#9729174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67746133-C-A

9729174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67746133-C-T

http://identifiers.org/hco/17/GRCh38#9729175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67746132-C-A

9729316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67746003-G-T

9729336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67745981-C-G

http://identifiers.org/hco/17/GRCh38#9729342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67745975-C-A

9729342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 67745975-C-T

http://identifiers.org/hco/17/GRCh38#9729347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#67745970-C-A

9729488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3 prime UTR variant
orthologous variants: 67745736-T-A

9729488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3 prime UTR variant
orthologous variants: 67745736-T-G

9729492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20072
most severe consequence: 3 prime UTR variant
orthologous variants: 67745732-G-T