31206289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5487773-G-T

http://identifiers.org/hco/10/GRCh38#31206320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5487786-C-A

31206386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5487874-C-T

31206440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5487932-C-G

31206906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5488045-C-G

31214773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5489060-T-C

31215157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5489389-C-G

31215193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5489429-G-A

31215413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5489664-A-G

http://identifiers.org/hco/10/GRCh38#31215425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5489676-C-A

31215488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5489804-T-C

31215528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5489890-C-T

http://identifiers.org/hco/10/GRCh38#31215860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5490207-C-A

31215860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490207-C-T

31216119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490468-G-C

31216120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490469-G-T

31216210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5490552-T-C

31216433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491355-C-T

http://identifiers.org/hco/10/GRCh38#31216533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5491475-C-A

31216553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491495-G-A

31216586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491536-G-A

31216726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491683-A-G

31216743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491699-T-C

31216764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491716-T-C

31216773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5491725-C-T

31218596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5493879-A-G

31218681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5493963-C-T

http://identifiers.org/hco/10/GRCh38#31218943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5494148-A-C

31219221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494415-T-C

31219367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494570-T-G

31219439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494641-G-A

31219439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494641-G-C

http://identifiers.org/hco/10/GRCh38#31219641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5494817-C-A

31219641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494817-C-T

31219648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5494824-A-G

31222898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5496627-C-T

31223025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5496733-T-C

31223102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5496802-C-G

31223244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5496901-C-T

31223766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5497695-C-T

31224084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5497916-T-A

31224084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5497916-T-C

31224216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498042-A-G

31224217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498043-T-A

31224217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498043-T-C

31224656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498259-A-G

31224703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498306-C-T

31224728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498325-T-C

31225058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498560-C-G

31225216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498673-G-A

31225216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498673-G-C

31225522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498902-C-T

31225523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5498903-G-A

31225739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5499094-G-A

31239589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506027-A-T

31239660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506097-A-G

31240149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5506951-G-A

http://identifiers.org/hco/10/GRCh38#31240332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5507146-C-A

31240332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507146-C-G

31240370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507177-G-A

31241020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507763-C-G

31241020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5507763-C-T

31241379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508105-T-C

31241493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508217-G-A

31241625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508348-C-T

http://identifiers.org/hco/10/GRCh38#31241738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5508446-C-A

31241738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508446-C-T

31241808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508514-A-G

31241832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508536-T-C

31242017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508673-G-A

31242017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5508673-G-T

31242449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509399-G-A

31242467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509417-G-T

http://identifiers.org/hco/10/GRCh38#31242722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5509789-C-A

31242724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509791-G-A

31242725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5509792-G-A

31242859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5510098-G-T

31242982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5510209-T-C

http://identifiers.org/hco/10/GRCh38#31243252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#5510448-A-C

31243252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5510448-A-T

31243273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5510469-A-T

http://identifiers.org/hco/10/GRCh38#31243374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#5510527-A-C

31243540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5510672-T-C

31243574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5510706-T-G

31243601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5510733-G-T

31259647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5514119-A-G

http://identifiers.org/hco/10/GRCh38#31259721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5514152-C-A

31259809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514233-T-C

31259893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5514320-T-C

http://identifiers.org/hco/10/GRCh38#31259984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5514408-C-A

31261135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515103-A-G

31261135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515103-A-T

31261139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515107-G-T

http://identifiers.org/hco/10/GRCh38#31261152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5515120-C-A

31261167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515135-G-C

31261255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515221-G-T

31261257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515223-A-T

http://identifiers.org/hco/10/GRCh38#31261282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5515274-C-A

31261880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5515873-G-A

http://identifiers.org/hco/10/GRCh38#31261988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5515981-C-A

31262030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5516019-T-C

31262223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5516210-G-A

31262597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5516592-A-G

31262726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5516714-A-T

31263121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5517086-G-C

31263254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5517218-C-T

31263383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5517355-G-C

31263628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5517523-C-T

31264073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5517898-A-T

31264375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5518142-T-A

http://identifiers.org/hco/10/GRCh38#31264562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5518308-C-A

31264610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5518357-G-A

http://identifiers.org/hco/10/GRCh38#31264668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5518405-C-A

31264668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5518405-C-T

31265323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5520762-T-C

31266696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523174-G-A

31266778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523253-T-C

31266798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523271-T-C

31266926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523436-T-A

31266948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5523459-C-T

http://identifiers.org/hco/10/GRCh38#31267238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5523780-C-A

31268538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525056-G-A

31268970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525464-G-C

31269081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525572-C-G

31269081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525572-C-T

31269133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525616-T-G

31269263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525745-G-C

31269291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525789-C-T

31269294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5525792-G-A

31269962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5526602-A-T

31271111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5533988-T-C

31271541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5535025-G-A

31274410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5537935-G-A

http://identifiers.org/hco/10/GRCh38#31274475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5537999-C-A

31274477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5538001-T-C

31274584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538106-A-G

31274648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5538172-T-G

http://identifiers.org/hco/10/GRCh38#31275461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5540577-C-A

31275498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5540614-G-A

31275516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5540632-C-T

31275854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5541237-C-T

31275963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5541341-T-A

31275963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5541341-T-C

31276393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5541718-T-C

31276462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5541780-T-A

31276468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5541786-A-T

31277086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5542349-T-C

31277475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5542728-C-G

31278758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5544537-T-G

31279226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545122-G-A

31279396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545285-G-A

http://identifiers.org/hco/10/GRCh38#31279469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5545353-A-C

31279469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545353-A-G

31279491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545376-G-A

31279503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545388-A-G

31279597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545467-G-A

31279798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545632-G-A

31279992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5545898-T-A

31280146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5546036-A-T

31280273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5546142-G-A

31294044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5561435-T-G

http://identifiers.org/hco/10/GRCh38#31294190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5561698-C-A

31294217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5561725-G-A

31294778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562710-A-G

31294894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562824-G-A

31294987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5562905-T-C

31295151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5563053-G-A

31295633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564155-A-G

31295645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564167-C-G

31295656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564174-T-C

31295709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564228-A-G

31295767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564282-T-C

31295785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564300-G-C

31295874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564388-C-T

31295909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564423-C-T

31295997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564491-A-G

31296268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564740-A-G

31296298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5564762-A-G

31296642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5565267-C-G

http://identifiers.org/hco/10/GRCh38#31296824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5565482-A-C

31297195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5565791-T-A

31297195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5565791-T-C

31300056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5567730-A-G

31300163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5567830-G-T

31300222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5567902-G-A

http://identifiers.org/hco/10/GRCh38#31300232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5567912-C-A

31300257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5567938-G-T

31300433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5568099-A-T

31300727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5568343-C-G

31300925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5568521-G-A

http://identifiers.org/hco/10/GRCh38#31301300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5568818-C-A

http://identifiers.org/hco/10/GRCh38#31301769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5569253-C-A

31301966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5569459-T-G

31301967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5569460-G-A

http://identifiers.org/hco/10/GRCh38#31302035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5569504-C-A

31302077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5569551-C-T

31302128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5569612-T-C

31302646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5570674-T-G

31302780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5570710-C-G

31303203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5571158-G-A

31303203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5571158-G-C

31303256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5571211-G-A

31303263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5571216-T-C

31303405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5571355-T-C

31303620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5571589-A-T

31304057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572055-A-T

31304419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572413-G-A

31304489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572480-T-C

31304695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572622-T-C

31304797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572710-T-C

http://identifiers.org/hco/10/GRCh38#31304882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5572790-A-C

31304882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572790-A-G

31304977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5572903-G-C

31305223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5573148-T-C

31305223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5573148-T-G

31311273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5584615-C-T

31311285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5584627-T-A

31311288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5584630-T-C

http://identifiers.org/hco/10/GRCh38#31311360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5584673-A-C

31311395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5584711-C-T

31311632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5584924-T-C

31311645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5584937-G-A

http://identifiers.org/hco/10/GRCh38#31312152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5585189-C-A

31312212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5585243-T-A

31312478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5585473-T-A

31312506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5585502-C-T

31313073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5585747-T-C

31313074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5585748-A-G

31313782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586112-T-C

31313858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586172-C-T

31314236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586479-G-T

31314267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586509-T-C

31314475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586684-T-C

31314475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586684-T-G

31314544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586750-G-T

31314554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586758-G-C

31314554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586758-G-T

31314561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586765-T-A

31314789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5586989-T-C

31315178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5587362-T-G

31315474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5587600-A-T

http://identifiers.org/hco/10/GRCh38#31315494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5587620-C-A

31315859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5588783-C-T

31315934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5588855-G-A

31315941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5588862-A-G

31315973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5588871-T-C

31316192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5589056-C-T

31316230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5589095-T-A

http://identifiers.org/hco/10/GRCh38#31316238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5589103-A-C

31316320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5589166-T-C

31316502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5589441-G-A

http://identifiers.org/hco/10/GRCh38#31316651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5589584-C-A

31316717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589643-T-A

http://identifiers.org/hco/10/GRCh38#31316785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5589717-A-C

31316819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589746-A-G

31316952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589870-T-A

31316952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589870-T-C

31316960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589879-T-C

31316991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589910-T-C

31317040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5589956-G-C

31317267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590150-G-T

31317326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590191-T-C

31317342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590207-T-C

31317383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590266-T-A

31317411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590303-C-T

31317412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590304-C-T

31317479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590363-T-C

http://identifiers.org/hco/10/GRCh38#31317740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5590585-A-C

31317899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590776-T-C

31317969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5590835-C-T

31318215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5591031-C-T

31318242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5591082-G-A

http://identifiers.org/hco/10/GRCh38#31318401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#5591254-C-A

31318576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5591408-G-T

http://identifiers.org/hco/10/GRCh38#31318602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#5591428-C-A

31318602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5591428-C-T

31318694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5591457-G-A

31318800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5591520-G-A

31318800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5591520-G-C

31318800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5591520-G-T

31319031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5591697-G-A

31319031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5591697-G-T

31319188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5591853-G-A

31319188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5591853-G-T

31319915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5592424-G-C

http://identifiers.org/hco/10/GRCh38#31319981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#5592485-C-A

31319981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5592485-C-T

31320148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5592590-C-T

31320427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42354
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 5592807-G-T