31400516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12936029-C-T

31400600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935966-T-C

31400636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935934-A-G

http://identifiers.org/hco/5/GRCh38#31400798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935795-C-A

31400798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935795-C-T

http://identifiers.org/hco/5/GRCh38#31400906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935689-A-C

31400906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935689-A-T

http://identifiers.org/hco/5/GRCh38#31400921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935674-C-A

31400921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935674-C-G

31400921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935674-C-T

http://identifiers.org/hco/5/GRCh38#31400993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935620-C-A

31400993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: 12935620-C-G

http://identifiers.org/hco/5/GRCh38#31401041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935573-A-C

31401156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12935464-C-T

31401349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12935287-C-G

31401349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12935287-C-T

http://identifiers.org/hco/5/GRCh38#31401520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935118-C-A

31401520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12935118-C-T

31401622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12935022-G-A

31401622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12935022-G-T

http://identifiers.org/hco/5/GRCh38#31401638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935013-C-A

31401642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12935009-T-A

31401642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12935009-T-C

31401642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12935009-T-G

http://identifiers.org/hco/5/GRCh38#31401643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12935008-A-C

31401643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12935008-A-G

31401662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12934989-C-T

http://identifiers.org/hco/5/GRCh38#31401697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12934952-C-A

31401719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12934928-C-T

31401975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12934661-T-C

31401987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12934649-A-G

31402100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12934537-A-G

31402143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12934495-T-A

31402357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12932137-C-T

31403291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12931928-A-G

31403388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12931836-T-C

31403417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12931806-A-G

31403514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12931732-T-C

31403550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12931693-A-G

http://identifiers.org/hco/5/GRCh38#31404252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12931160-C-A

31404402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12930965-C-T

31404554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12930809-C-T

31404968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12930433-T-C

31404968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12930433-T-G

http://identifiers.org/hco/5/GRCh38#31405408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12930005-C-A

31405547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929914-G-C

31405547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929914-G-T

31405598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929865-T-C

31405651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929821-A-G

http://identifiers.org/hco/5/GRCh38#31405652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12929820-A-C

31405652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929820-A-T

31405658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929814-G-A

31405658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929814-G-T

http://identifiers.org/hco/5/GRCh38#31405730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12929742-A-C

31405730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12929742-A-T

31405783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929709-T-A

31405783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929709-T-C

http://identifiers.org/hco/5/GRCh38#31405814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12929693-C-A

31405814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929693-C-T

31406013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929500-G-A

31406552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929304-A-G

31406639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929238-G-A

31406652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929227-A-G

http://identifiers.org/hco/5/GRCh38#31406726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12929149-C-A

31406730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12929145-T-C

http://identifiers.org/hco/5/GRCh38#31406773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12929104-C-A

http://identifiers.org/hco/5/GRCh38#31407003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12928895-A-C

31407003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12928895-A-G

31407013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12928886-G-A

31407013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12928886-G-T

31407386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12928486-T-G

31407680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12928198-G-A

31407900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12928001-T-A

31407900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12928001-T-C

31408703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926669-A-G

31408721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12926651-G-A

31408742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12926636-A-G

31408781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12926600-T-C

http://identifiers.org/hco/5/GRCh38#31408794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12926587-C-A

31408990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12926451-G-A

31408990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12926451-G-T

31409018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12926426-T-C

31409308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12926099-T-A

31409359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12926052-A-G

31409377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12925981-T-C

31409441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12925839-G-T

31409494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12925792-T-A

31409535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12925756-A-G

http://identifiers.org/hco/5/GRCh38#31409550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12925743-A-C

http://identifiers.org/hco/5/GRCh38#31409594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12925695-C-A

31409594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925695-C-G

31409613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925471-A-G

http://identifiers.org/hco/5/GRCh38#31409658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12925421-C-A

31409658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925421-C-G

31409696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925383-C-T

31409888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925209-G-A

31410076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925065-A-G

31410089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12925052-A-G

31410190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924958-G-A

31410248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924897-T-C

31410412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924751-C-T

31410457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924684-T-C

31410609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924441-T-C

31410625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924419-T-G

31410641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924402-G-T

http://identifiers.org/hco/5/GRCh38#31410683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12924351-A-C

31410708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924325-T-C

31410787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12924240-G-A

31410897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924130-A-G

31410897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924130-A-T

31410909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924118-A-G

31410932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924095-T-C

31410955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924070-G-A

31410955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924070-G-T

http://identifiers.org/hco/5/GRCh38#31410970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12924055-A-C

31410970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12924055-A-T

31411291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12923742-C-T

31411431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12923607-A-T

http://identifiers.org/hco/5/GRCh38#31411657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12923408-C-A

31412012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12923195-G-C

31412125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12923090-G-C

31412801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12922398-G-A

31412904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12922323-G-C

31412904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12922323-G-T

31413010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12922231-T-C

31413135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12922106-A-G

31413304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921950-A-G

31413432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921823-T-C

31413432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921823-T-G

31413434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921821-A-G

http://identifiers.org/hco/5/GRCh38#31413460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12921795-A-C

31413589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921671-G-A

http://identifiers.org/hco/5/GRCh38#31413658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12921600-A-C

31413658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921600-A-G

31413658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921600-A-T

http://identifiers.org/hco/5/GRCh38#31413734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12921529-A-C

31413819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921457-A-G

31413890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921396-G-A

http://identifiers.org/hco/5/GRCh38#31413933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12921344-A-C

31414005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921272-G-T

31414061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921218-G-A

31414696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921040-C-T

31414704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12921032-G-A

31414772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920964-G-A

31414772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920964-G-T

31414839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920903-C-G

31415018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920742-A-T

31415064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920697-G-A

31415216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920578-A-G

31415515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920276-T-C

31415710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920079-C-G

31415710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12920079-C-T

31416004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919524-T-C

31416444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12919107-C-G

31417260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12918476-A-G

31417432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12918374-T-C

31417590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12918182-A-G

31417650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12918122-A-T

31417725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12918044-T-C

31418002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12917843-T-C

31418149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12917704-T-C

31418186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12917666-C-G

31418763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12917495-G-T

31418999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12917279-G-A

31419553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916679-G-T

31419568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916667-T-A

31419568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916667-T-C

31419568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916667-T-G

31419699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916565-C-T

31419987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12916313-A-G

31420476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915887-A-G

http://identifiers.org/hco/5/GRCh38#31420481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12915882-C-A

31420481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915882-C-T

31420515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915862-G-A

31420515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915862-G-C

http://identifiers.org/hco/5/GRCh38#31420573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12915810-A-C

http://identifiers.org/hco/5/GRCh38#31421171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12915636-C-A

31421191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915615-A-G

31421191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915615-A-T

http://identifiers.org/hco/5/GRCh38#31421192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12915614-C-A

31421192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915614-C-T

31421243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915557-T-C

31421421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12915379-T-C

http://identifiers.org/hco/5/GRCh38#31421435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12915349-A-C

31421869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 12914985-T-A

31421869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 12914985-T-C

31421869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 12914985-T-G

31421935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914942-T-A

31421935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914942-T-G

31421969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914923-A-G

31422134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914889-T-C

31422239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914796-G-A

31422279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914754-G-T

31422610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914309-T-C

31422638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914281-A-G

31422641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914278-G-T

http://identifiers.org/hco/5/GRCh38#31422662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12914262-C-A

31422662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914262-C-G

31422663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914261-T-A

31422668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914256-A-G

31422668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914256-A-T

31422702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12914223-A-G

31422865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12914062-A-G

http://identifiers.org/hco/5/GRCh38#31423178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12913751-C-A

31423178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12913751-C-G

http://identifiers.org/hco/5/GRCh38#31423265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12913668-A-C

31423265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12913668-A-G

31423298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12913657-T-G

http://identifiers.org/hco/5/GRCh38#31423300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12913655-C-A

31423300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12913655-C-T

31423360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913621-G-A

31423368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913613-A-G

http://identifiers.org/hco/5/GRCh38#31423389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12913592-C-A

31423425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913558-T-A

31423428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913555-G-A

31423610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913364-G-T

31423868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913128-T-C

31423961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12913040-T-G

31424014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912996-T-C

31424174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912854-T-C

http://identifiers.org/hco/5/GRCh38#31424293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12912757-A-C

31424353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912698-A-G

31424464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12912602-C-T

31424484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912582-G-A

31424484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912582-G-T

31424682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12912387-C-T

http://identifiers.org/hco/5/GRCh38#31424764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12912143-C-A

31425005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911940-G-C

http://identifiers.org/hco/5/GRCh38#31425420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12911539-C-A

31425502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911440-C-T

31425504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911438-C-T

31425609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911347-G-C

31425735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12911238-C-T

31426890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12909954-G-A

31427241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12909614-T-C

http://identifiers.org/hco/5/GRCh38#31427985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12908830-C-A

31428087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908730-T-C

31428404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12908467-T-C

31429357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907578-A-G

31429357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907578-A-T

31429368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907568-G-A

31429368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907568-G-T

31429437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907517-T-C

31429606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907347-T-C

31429816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12907152-T-G

http://identifiers.org/hco/5/GRCh38#31430077-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12906996-A-C

31430923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12906408-T-A

31431406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905937-T-A

31431406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905937-T-C

31431428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905913-T-A

31431428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905913-T-C

31431444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905897-G-C

31431444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905897-G-T

http://identifiers.org/hco/5/GRCh38#31431490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12905864-C-A

31431512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905842-T-C

31431513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905841-A-G

31431538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905815-T-C

31431538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905815-T-G

31431650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12905711-T-C

31431740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905635-T-A

31431741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905634-C-T

31431795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905581-T-C

31431821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905575-G-A

31431821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905575-G-C

31431821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905575-G-T

31432812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12905294-T-G

31433430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904771-G-A

31433564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904682-A-T

31433565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904681-G-T

31433569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904677-G-C

31433569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904677-G-T

31433571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904675-G-A

31433578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904670-T-C

31433598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904646-G-C

31433598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12904646-G-T

31434985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12903537-A-T

31435335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12903162-T-C

http://identifiers.org/hco/5/GRCh38#31435397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12903092-A-C

31435397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12903092-A-G

31435569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902946-T-C

http://identifiers.org/hco/5/GRCh38#31435623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12902910-C-A

31435623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902910-C-G

31435623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902910-C-T

31435685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902841-T-G

31435748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902786-G-C

http://identifiers.org/hco/5/GRCh38#31435869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12902664-A-C

31435869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12902664-A-G

31435896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902634-T-C

31435928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902605-G-T

http://identifiers.org/hco/5/GRCh38#31435938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12902595-C-A

31435938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902595-C-G

31435938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902595-C-T

http://identifiers.org/hco/5/GRCh38#31435939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12902594-A-C

31435939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902594-A-G

http://identifiers.org/hco/5/GRCh38#31435947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12902591-C-A

31435947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902591-C-T

31436219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12902174-T-C

http://identifiers.org/hco/5/GRCh38#31436226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12902167-C-A

31436734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901764-G-A

31436761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901727-C-T

31436777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901711-C-T

31436793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901695-C-G

31436798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901690-T-A

31436946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901533-G-A

31437214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901276-G-A

31437214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901276-G-C

31437214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12901276-G-T

31437311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12901175-T-C

31437321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12901165-T-G

http://identifiers.org/hco/5/GRCh38#31437330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12901156-C-A

31437523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12900366-C-G

31437917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12900000-G-A

31441042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12899669-G-A

31441043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12899668-G-A

31441412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12899455-A-G

31441783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12898741-T-C

31441868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12898654-T-C

http://identifiers.org/hco/5/GRCh38#31442109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12898421-A-C

31442190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12898344-T-C

31442435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12897858-T-C

31442457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12897837-C-T

31442513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12897788-C-T

31444712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12894982-G-A

31444762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12894933-T-G

31444767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12894928-A-G

31444788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12894907-G-C

31445194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12893705-T-C

31445215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12893684-C-T

31448170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890964-T-G

31448251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890900-A-G

31448364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890809-G-C

31448452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890723-T-C

31448469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890703-T-C

31448556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12890622-G-A

31449181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890326-A-G

31449181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890326-A-T

31449202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890308-T-A

31449202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890308-T-C

31449247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890285-A-G

31449247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890285-A-T

31449250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890282-A-G

31449256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12890281-A-G

31451461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889884-A-G

31451462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889883-C-T

31451466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889879-T-C

31451498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889847-G-T

31451672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889674-T-C

31451675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889671-T-A

31451675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889671-T-C

31451702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889646-T-C

31451788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889560-A-G

31451866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889478-T-A

31451914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889437-C-T

31451930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12889424-C-T

31452456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888454-T-C

31452561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888350-G-A

31452648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888265-T-C

31452718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888193-C-T

31452724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888187-A-T

http://identifiers.org/hco/5/GRCh38#31452751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12888163-C-A

31452811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888103-C-G

31452811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12888103-C-T

31452909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12887997-T-C

31463013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886375-G-T

31463091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12886291-G-A

31463435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885939-T-C

31463853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885564-C-T

31463908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885508-A-G

31463972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885457-A-G

http://identifiers.org/hco/5/GRCh38#31463983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12885451-C-A

31464024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885397-A-G

http://identifiers.org/hco/5/GRCh38#31464026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12885395-C-A

31464026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885395-C-T

31464093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12885313-G-A

31464093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12885313-G-C

31464102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12885304-T-A

31464102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12885304-T-C

http://identifiers.org/hco/5/GRCh38#31464149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12885262-C-A

31464149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12885262-C-T

http://identifiers.org/hco/5/GRCh38#31464155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12885256-C-A

31464420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12885000-T-C

31464525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884892-G-A

31464533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884884-C-G

31464576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884847-A-G

31464582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884841-T-C

31464817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884498-C-T

http://identifiers.org/hco/5/GRCh38#31465000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12884358-C-A

31465029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884312-C-T

31465065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884280-G-A

31465080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12884265-G-A

31465422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883979-T-G

31465553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883855-A-G

31466092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883437-T-C

31466108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883421-T-C

http://identifiers.org/hco/5/GRCh38#31466118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12883411-C-A

31466118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883411-C-T

31466161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883369-G-A

31466339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12883192-C-G

http://identifiers.org/hco/5/GRCh38#31466376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12883163-C-A

31466376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12883163-C-T

31466470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12883079-A-G

31466470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12883079-A-T

31466504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12883045-T-C

31466618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882923-A-G

31466733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882838-A-G

31466799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882773-G-A

31466799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882773-G-C

31467074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882580-G-A

31467082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882573-C-T

31467147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882519-G-A

31467147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882519-G-T

31467358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882334-C-T

31467402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12882295-T-A

http://identifiers.org/hco/5/GRCh38#31467428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12882268-C-A

31467492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882197-C-G

31467514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882174-G-C

31467661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882054-A-G

http://identifiers.org/hco/5/GRCh38#31467667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12882048-C-A

31467667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882048-C-T

31467682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12882033-A-G

31467719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12881998-T-C

31467726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12881991-T-C

31467866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12881902-G-T

31467882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12881888-A-G

31467897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12881873-G-T

http://identifiers.org/hco/5/GRCh38#31468117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12881649-C-A

http://identifiers.org/hco/5/GRCh38#31468173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12881594-C-A

31468173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881594-C-G

31468481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881294-T-C

31468558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881226-T-C

31468562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12881215-C-T

31469842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880381-T-C

31469991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880211-G-A

31469991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880211-G-T

31470024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12880182-C-T

31470408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879849-C-T

31470675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879674-T-C

31470699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879654-T-C

http://identifiers.org/hco/5/GRCh38#31470700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12879653-C-A

31470706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879647-G-A

31470706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879647-G-T

31470716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879637-A-T

31471835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12879110-T-A

31471999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878975-T-A

31471999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878975-T-C

31471999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878975-T-G

http://identifiers.org/hco/5/GRCh38#31472046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12878928-C-A

31472046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878928-C-G

31472046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878928-C-T

http://identifiers.org/hco/5/GRCh38#31472341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12878647-C-A

31472341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878647-C-T

31472554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878447-C-T

31472651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878351-T-C

31472773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878230-C-G

31472795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12878208-T-C

31473054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12877971-A-G

31475860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876638-T-C

31476467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876332-A-G

31476509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876287-C-T

31476697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12876134-G-A

31476844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875988-T-C

31476860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875972-C-G

31476860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875972-C-T

31477326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12875515-T-C

31477917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12874622-A-G

31478955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12873761-G-A

31479074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12873637-T-C

31481272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869635-G-A

31481749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869200-T-C

31481750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869199-T-G

31481885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869051-C-T

http://identifiers.org/hco/5/GRCh38#31482095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12868868-C-A

http://identifiers.org/hco/5/GRCh38#31482244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12868780-C-A

31482244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868780-C-G

31482579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868544-T-C

31482623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868500-G-A

http://identifiers.org/hco/5/GRCh38#31482792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12868360-C-A

31483186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868123-T-C

31483407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867901-A-G

31483407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867901-A-T

31483469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867839-T-C

31483470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867838-T-C

http://identifiers.org/hco/5/GRCh38#31483482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12867826-C-A

31483482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867826-C-T

http://identifiers.org/hco/5/GRCh38#31483497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12867811-C-A

31483497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867811-C-G

31483497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867811-C-T

31483675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867634-T-A

31483675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867634-T-C

31483829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867485-A-G

http://identifiers.org/hco/5/GRCh38#31483830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12867484-C-A

31483888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867428-C-T

31483949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867366-C-T

31483981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867337-C-G

31484399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867176-A-T

http://identifiers.org/hco/5/GRCh38#31484419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12867156-A-C

31484491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867130-G-A

31484491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867130-G-T

31484618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866998-A-G

31484730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866863-A-T

31484794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866801-T-A

31484794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866801-T-C

31484801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866794-A-G

http://identifiers.org/hco/5/GRCh38#31484927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12866682-C-A

31484927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12866682-C-G

31484927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12866682-C-T

31485053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866570-G-A

31485053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866570-G-C

31485053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866570-G-T

31485212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866388-G-A

http://identifiers.org/hco/5/GRCh38#31485471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12866129-A-C

http://identifiers.org/hco/5/GRCh38#31485546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12866071-A-C

31485952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865731-A-G

31486044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865639-A-G

31486239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865449-T-A

31486239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865449-T-C

31486651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865028-G-C

31486651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865028-G-T

31486697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12864791-T-C

http://identifiers.org/hco/5/GRCh38#31486759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12864730-C-A

31486759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864730-C-T

http://identifiers.org/hco/5/GRCh38#31486761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12864728-C-A

31486779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864711-G-A

31486779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12864711-G-C

http://identifiers.org/hco/5/GRCh38#31486877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12864612-C-A

31487962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12863566-A-G

http://identifiers.org/hco/5/GRCh38#31490686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12863066-C-A

http://identifiers.org/hco/5/GRCh38#31490704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12863048-C-A

31492732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12862307-A-G

31492732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12862307-A-T

http://identifiers.org/hco/5/GRCh38#31493070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12861980-C-A

31493086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12861970-C-T

31493103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12861953-A-G

31493155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12861893-G-T

31493315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12861740-A-G

31493759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12861675-C-T

31495299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12859530-G-T

http://identifiers.org/hco/5/GRCh38#31495448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12859381-A-C

http://identifiers.org/hco/5/GRCh38#31495752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12859052-C-A

31495752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12859052-C-T

31495903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858909-G-C

31495983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858864-A-G

31496052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858827-T-C

31496064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858815-G-A

31496096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858783-G-A

31496509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858665-T-C

31496536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858636-G-A

31496633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858547-A-G

31496766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858459-A-G

31496796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858430-G-A

31496798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858428-G-A

31497208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12858036-C-T

31497648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12857212-G-T

http://identifiers.org/hco/5/GRCh38#31498116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12856778-C-A

http://identifiers.org/hco/5/GRCh38#31499557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12856481-A-C

31499557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12856481-A-G

31499617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12856437-G-A

31499820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12856109-G-A

31499828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12856101-C-T

31499879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12856040-A-G

31499893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12856026-G-A

31499995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855884-T-C

31500208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855664-C-T

31500344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855559-G-A

31500470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855483-C-T

31500672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855324-A-G

31500947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855290-G-A

31500963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855274-G-T

31501044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855193-A-T

31501090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855145-C-T

http://identifiers.org/hco/5/GRCh38#31501140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12855092-C-A

31501235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12855001-C-T

31501359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854906-C-G

31501491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854776-A-G

31501533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854735-C-T

31501557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854719-G-A

31501586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854702-A-G

http://identifiers.org/hco/5/GRCh38#31502033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12854292-C-A

31502033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854292-C-T

31502197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12854137-A-G

31502366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853976-C-T

31502388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853959-T-C

31502638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853746-C-T

31502651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853732-A-G

31502774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853635-G-A

31502803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853606-G-A

31503223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853303-G-C

31503237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12853289-G-T

31503568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852933-C-G

31503637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852865-G-A

31503826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852686-A-G

31504145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852404-T-C

31504237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852286-C-T

31504404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852132-G-A

31504404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852132-G-T

31504448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852066-A-G

31504448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852066-A-T

http://identifiers.org/hco/5/GRCh38#31504471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12852041-C-A

31504486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852026-G-A

31504486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12852026-G-T

http://identifiers.org/hco/5/GRCh38#31504515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12851999-C-A

31504515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12851999-C-T

31504547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12851968-C-T

http://identifiers.org/hco/5/GRCh38#31504691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12851827-A-C

31504701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12851817-C-T

31504813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12851737-T-C

31505090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12851435-A-G

31505092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12851433-T-C

http://identifiers.org/hco/5/GRCh38#31505485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12851072-C-A

31505510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12851048-G-T

31505808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12850487-C-T

31505929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12850373-T-C

31506820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12850177-C-T

31506839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12850159-G-A

http://identifiers.org/hco/5/GRCh38#31508313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12848590-C-A

31508561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12848352-G-A

31508780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12848132-C-G

31508782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12848130-G-C

31508785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12848127-G-T

31508813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12848097-A-G

31509864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12847354-T-C

31509979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12847256-A-G

31510040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12847200-T-A

31510243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12847107-C-T

31510396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12847015-G-A

31510651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12846641-C-T

31510848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12846392-T-C

31510981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12846338-A-T

31511209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12846119-A-G

31511209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12846119-A-T

http://identifiers.org/hco/5/GRCh38#31513314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12844769-C-A

31513314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12844769-C-T

31513621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12844688-C-T

31514691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12843294-C-T

31514759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12843228-G-T

31514805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842788-T-C

31514844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842749-A-G

31514853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842740-A-T

31514879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842714-A-G

31514879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842714-A-T

31514887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842706-T-C

http://identifiers.org/hco/5/GRCh38#31514892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12842701-C-A

31514892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842701-C-T

http://identifiers.org/hco/5/GRCh38#31514897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12842700-C-A

31514897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842700-C-T

31514900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842697-A-G

31514922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842676-C-T

31514928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842670-G-A

31514928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842670-G-T

http://identifiers.org/hco/5/GRCh38#31514942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12842656-C-A

31514942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842656-C-T

http://identifiers.org/hco/5/GRCh38#31514952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12842648-C-A

31514954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842646-C-G

http://identifiers.org/hco/5/GRCh38#31514959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12842641-C-A

31514959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842641-C-G

31514962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842638-C-T

31515064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12842539-T-C

31515064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12842539-T-G

http://identifiers.org/hco/5/GRCh38#31515078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12842525-A-C

31515078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: synonymous variant
orthologous variants: 12842525-A-G

31515085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12842518-T-A

31515092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12842511-T-C

31515121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12842482-G-A

31515390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842311-G-T

31515472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, missense_variant
orthologous variants: 12842233-G-T

31515511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, missense_variant
orthologous variants: 12842194-G-C

31515511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, missense_variant
orthologous variants: 12842194-G-T

31515549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 12842156-C-T

31515577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842128-G-A

31515577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842128-G-T

31515624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842081-A-G

31515697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12842008-A-G

31515777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12841932-G-C

31515797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12841913-G-C

http://identifiers.org/hco/5/GRCh38#31519581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12839364-A-C

31519673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12839272-T-C

31519675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12839270-A-G

31519928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12839046-C-T

31519929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12839045-G-A

31519969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12839017-G-A

31520130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12838871-T-A

31520133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12838868-T-C

31520236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12838744-T-A

31520408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12838141-C-T

31520462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12838092-G-A

31520475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12838079-T-C

http://identifiers.org/hco/5/GRCh38#31520550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12838015-C-A

31520584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837969-T-A

31520631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837921-C-T

31520742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837828-T-C

31520783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837787-G-A

31520940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837589-T-C

http://identifiers.org/hco/5/GRCh38#31520985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12837568-C-A

31521038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837522-A-G

31521038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837522-A-T

http://identifiers.org/hco/5/GRCh38#31521259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12837325-C-A

31521259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837325-C-T

31521316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837272-G-A

31521316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837272-G-T

31521371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12837228-G-A

31521728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12836987-A-G

31522192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12836428-T-C

http://identifiers.org/hco/5/GRCh38#31522492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12836179-A-C

31522613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12836032-A-T

31522616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12836029-T-C

31522952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12835705-C-T

31525823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12835107-C-T

31525888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12835056-G-C

31525953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12834997-T-C

http://identifiers.org/hco/5/GRCh38#31525986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12834949-C-A

31525986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12834949-C-G

31525986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron variant
orthologous variants: 12834949-C-T

31526127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834695-T-C

http://identifiers.org/hco/5/GRCh38#31526141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12834681-C-A

31526141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: synonymous variant
orthologous variants: 12834681-C-T

31526247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834575-T-C

31526397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834425-G-A

31526466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834359-G-A

31526466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834359-G-T

31526473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834352-G-A

31526473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834352-G-T

31526591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: synonymous variant
orthologous variants: 12834234-A-T

http://identifiers.org/hco/5/GRCh38#31526709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12834116-C-A

31526709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834116-C-G

31526709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense variant
orthologous variants: 12834116-C-T

31526790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12834035-G-A

31526796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12834029-T-C

31526796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12834029-T-G

31526907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: missense_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 12833918-C-G

31526980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12833245-T-G

http://identifiers.org/hco/5/GRCh38#31527373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12830036-C-A

31527373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830036-C-T

31527471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829945-A-G

31527498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829918-A-G

http://identifiers.org/hco/5/GRCh38#31527523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12829900-C-A

31527523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12829900-C-T

http://identifiers.org/hco/5/GRCh38#31527526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12829897-A-C

31527526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12829897-A-G

31528726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827691-T-G

31528750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827667-A-G

http://identifiers.org/hco/5/GRCh38#31528811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12827607-A-C

31528820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827598-G-A

31528899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827511-T-C

31528921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827489-G-T

http://identifiers.org/hco/5/GRCh38#31528943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12827467-A-C

31528943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827467-A-G

31529057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 12827359-C-T

http://identifiers.org/hco/5/GRCh38#31529183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12827215-C-A

31529183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827215-C-G

31529183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12827215-C-T

http://identifiers.org/hco/5/GRCh38#31529795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12826938-C-A

31530058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826690-C-G

31530058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826690-C-T

31530384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826538-T-C

31530530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826386-C-T

31530687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826355-T-A

http://identifiers.org/hco/5/GRCh38#31530788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12826261-C-A

31530807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12826242-C-T

http://identifiers.org/hco/5/GRCh38#31530862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12826195-C-A

31530968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12826106-T-C

31531062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12826001-G-A

31531077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12825986-G-A

31531095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825968-T-C

31531451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 12825476-T-C

31531518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12825428-G-A

31531518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12825428-G-T

31531578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825372-G-A

31531578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825372-G-T

31531661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12825294-A-T

31531760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825202-T-G

http://identifiers.org/hco/5/GRCh38#31531960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#12825058-C-A

31532005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12825011-G-T

31532048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12824973-A-G

31532048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12824973-A-T

http://identifiers.org/hco/5/GRCh38#31532055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#12824966-A-C

31532055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12824966-A-G

31532122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 12824899-G-A

31532122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 12824899-G-T

31532125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 12824896-G-A

31532125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 12824896-G-T

http://identifiers.org/hco/5/GRCh38#31532164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17904
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#12824855-C-A