149271881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919738-G-A

149271881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919738-G-T

http://identifiers.org/hco/5/GRCh38#149271901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61919719-C-A

149271901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61919719-C-T

http://identifiers.org/hco/5/GRCh38#149271904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61919716-C-A

149271904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61919716-C-T

149271924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919705-G-A

149271924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919705-G-C

149271924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919705-G-T

149271937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919692-G-A

149271937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919692-G-C

149271937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919692-G-T

http://identifiers.org/hco/5/GRCh38#149271961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61919668-C-A

149271961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61919668-C-T

149272118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919551-G-A

149272118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919551-G-T

149272121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919548-A-G

149272224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61919425-G-C

149272294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919371-T-C

149273085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919092-C-G

149273085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919092-C-T

149273370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918865-T-A

149273417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918815-C-G

http://identifiers.org/hco/5/GRCh38#149273803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61918536-C-A

149273803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918536-C-T

149273903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918448-C-T

149274170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61918260-A-G

149276093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61916482-T-G

149276362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61916287-A-G

149276416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61916237-A-G

149279129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915896-G-A

149279413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915491-C-G

149279413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915491-C-T

149279499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915403-G-T

149279558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915344-T-C

149279585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915314-G-A

149279585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915314-G-T

149279603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915296-C-T

149279759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915003-A-T

149279975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61914802-C-G

http://identifiers.org/hco/5/GRCh38#149280003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61914771-C-A

149280101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61914673-G-A

149280438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61914330-A-G

149280553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61914225-T-A

149281152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61913615-T-C

149281152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61913615-T-G

149281260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61913510-T-C

149281441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61913336-C-T

149281740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61912206-T-C

149281831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61912161-G-A

149281894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61912104-T-A

149281927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61912067-A-G

149282081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61911941-T-C

149282146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61911878-C-T

http://identifiers.org/hco/5/GRCh38#149282248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61911774-C-A

149282596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61911427-G-A

149283139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61910553-T-C

149283228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61910474-A-G

149283612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61910107-C-T

149287430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901708-A-G

149288502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901199-T-C

149288504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901197-G-A

149288504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901197-G-T

149289331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61900435-C-T

149289713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61900085-G-T

149289775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61900035-G-A

149289793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61900019-G-A

149289813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61900002-G-A

149289962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899887-G-A

149289962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899887-G-C

149289985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899865-G-A

149290640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899217-A-G

149290657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899200-C-T

149290776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899092-C-T

149290779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899089-G-C

149290779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899089-G-T

149292291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61897241-G-A

149292638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896888-T-C

149292697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896838-A-G

149292776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896772-G-A

149292776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896772-G-C

149292817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896287-G-A

149293045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896096-T-C

149293341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895809-C-T

149293368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895788-G-A

149293417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895740-T-C

149293648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895559-T-C

149293897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895359-G-A

149293952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895302-T-G

149294161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895119-G-T

149297140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893804-A-G

149297224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893717-C-T

149297473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893525-A-G

149297930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893171-C-T

149298046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893083-G-A

149298372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892795-C-T

149298383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892784-T-C

149298386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892781-A-G

149298945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892288-G-A

149299110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892124-A-G

149299170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892087-A-G

149299254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892017-G-A

149299435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61891843-G-A

149299442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61891836-G-A

149299562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61891744-G-A

149299562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61891744-G-C

149299752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891598-T-A

http://identifiers.org/hco/5/GRCh38#149299754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61891597-C-A

149299754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891597-C-T

http://identifiers.org/hco/5/GRCh38#149299788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61891563-C-A

149299788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891563-C-T

149299817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891542-A-G

149299829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61891530-A-G

149299858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891502-C-T

149299869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891491-C-G

http://identifiers.org/hco/5/GRCh38#149299876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#61891484-C-A

149299876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891484-C-G

149299930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891408-A-G

149299947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891390-C-T

149299992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61891344-C-T

149300247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890829-G-A

149300251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890826-G-A

149300251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890826-G-T

149300252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890825-T-C

149300261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890816-T-G

149300477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890601-T-C

149300601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890510-C-T

149300628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890481-C-T

149300662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890445-C-T

149300714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890383-G-T

http://identifiers.org/hco/5/GRCh38#149300756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61890346-C-A

149300872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890222-C-G

149300894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890200-A-G

149300987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890114-A-G

149300988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890113-A-G

149300992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890109-T-A

149300992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61890109-T-G

149301126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61890010-T-A

http://identifiers.org/hco/5/GRCh38#149301329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61889836-C-A

149301333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889832-A-G

149301356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889811-T-A

149301362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889805-A-G

149301370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889797-G-A

149301370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889797-G-T

http://identifiers.org/hco/5/GRCh38#149301372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61889795-C-A

149301372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889795-C-T

149301377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889790-C-T

149301381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889786-G-T

149301382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889785-T-A

149301399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889768-C-T

149301568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889667-A-G

149301626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889583-A-G

149302199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889100-G-A

149302262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889039-T-A

149302262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61889039-T-C

149302296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888992-A-T

http://identifiers.org/hco/5/GRCh38#149302353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61888833-C-A

149302353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888833-C-T

http://identifiers.org/hco/5/GRCh38#149302378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61888805-C-A

149302378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888805-C-T

149302380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888803-G-A

149302380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888803-G-T

http://identifiers.org/hco/5/GRCh38#149302484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61888674-C-A

149302484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61888674-C-T

149302555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61888604-G-T

149302626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61888567-T-A

149302626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61888567-T-C

149302659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61888535-A-G

149302660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61888534-G-A

149302660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61888534-G-T

149302670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888524-T-C

149302712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888508-T-C

http://identifiers.org/hco/5/GRCh38#149302749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61888479-C-A

149302749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888479-C-G

http://identifiers.org/hco/5/GRCh38#149302770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61888458-A-C

149302770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888458-A-G

149302792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888435-T-A

149302792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888435-T-C

149302792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888435-T-G

149302835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888394-C-G

149302892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888345-T-C

149302912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888332-G-A

149302912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888332-G-C

149303197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888055-A-G

149303198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888054-T-C

149303544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887757-C-T

149303791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887230-A-G

149304107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886939-A-G

149304114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886932-G-A

149304123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886902-T-C

http://identifiers.org/hco/5/GRCh38#149304177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61886845-C-A

http://identifiers.org/hco/5/GRCh38#149304245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61886768-C-A

149304424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886605-A-G

149304448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886576-T-C

149304448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886576-T-G

149304537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886490-C-T

149304578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886468-G-A

149304594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886452-C-T

149304646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886396-T-C

http://identifiers.org/hco/5/GRCh38#149304734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61886315-C-A

149304734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886315-C-T

http://identifiers.org/hco/5/GRCh38#149304894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61886173-C-A

149304935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886140-T-C

http://identifiers.org/hco/5/GRCh38#149306243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885739-A-C

http://identifiers.org/hco/5/GRCh38#149306261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885721-C-A

149306261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885721-C-G

149306261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885721-C-T

http://identifiers.org/hco/5/GRCh38#149306286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885697-C-A

http://identifiers.org/hco/5/GRCh38#149306431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885551-C-A

149306478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885505-T-C

http://identifiers.org/hco/5/GRCh38#149306492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885491-C-A

149306492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885491-C-T

http://identifiers.org/hco/5/GRCh38#149306533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885418-C-A

149306533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885418-C-T

http://identifiers.org/hco/5/GRCh38#149306561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61885397-C-A

149306763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885251-T-G

149307342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885010-G-T

149307672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884703-T-C

149307778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884626-G-A

http://identifiers.org/hco/5/GRCh38#149307788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61884625-A-C

149307828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884571-C-G

149307956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884429-G-A

149308046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884340-G-A

149309652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61882171-G-A

149309812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61882039-T-C

http://identifiers.org/hco/5/GRCh38#149309834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61882020-C-A

149309998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61881902-G-C

149310013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61881887-A-G

149310013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61881887-A-T

149310088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61881812-T-G

149310193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881703-A-G

http://identifiers.org/hco/5/GRCh38#149310261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61881663-C-A

149310261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881663-C-T

149310296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881637-C-T

149310472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881471-A-G

149310847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881177-G-A

149310906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881118-C-T

http://identifiers.org/hco/5/GRCh38#149310979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61881046-A-C

149311222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880787-T-G

149311383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880634-G-A

149311441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880578-C-G

149311524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880522-G-A

http://identifiers.org/hco/5/GRCh38#149311964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61880084-C-A

149311964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880084-C-T

http://identifiers.org/hco/5/GRCh38#149312187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61879864-A-C

149312278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61879787-T-A

149313659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61879116-A-G

149313818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878947-G-A

149313959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878809-G-C

149313995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878780-T-C

149314052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878732-A-T

149314067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878717-G-A

149314109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878676-G-T

149314233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878564-T-A

149314239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878558-T-C

149314264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878499-T-C

149314304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878456-A-T

149314349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878339-G-A

149314349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61878339-G-T

149314682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877940-G-A

149314956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877683-T-C

149315193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877445-A-G

149315196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877442-A-T

149315220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877333-G-T

149315441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877120-T-C

149315524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877061-G-A

149315524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877061-G-T

149315532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron variant
orthologous variants: 61877055-T-C

149315674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61876938-G-C

149315674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61876938-G-T

http://identifiers.org/hco/5/GRCh38#149315752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61876889-C-A

149315752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61876889-C-T

149315781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61876868-A-G

149315782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 61876867-T-C

149315882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61876768-C-T

149315922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61876728-C-T

149315949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876691-T-G

149315984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876657-C-T

149316005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876645-T-C

149316007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876643-C-G

http://identifiers.org/hco/5/GRCh38#149316286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61876364-A-C

149316360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876288-G-A

149316592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876084-C-T

149317245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61875307-T-G

149317375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61875208-G-A

149317375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61875208-G-C

http://identifiers.org/hco/5/GRCh38#149317477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61875123-C-A

149317496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61875105-T-C

149317740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61874899-G-A

149317963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61874678-G-T

149317987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61874662-T-A

http://identifiers.org/hco/5/GRCh38#149318575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61874138-A-C

149318661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61874068-C-T

149319385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61872519-G-T

149319496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61872424-T-C

http://identifiers.org/hco/5/GRCh38#149319576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61872343-C-A

http://identifiers.org/hco/5/GRCh38#149319833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61872082-A-C

149319862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61872052-A-G

149320157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61871982-G-A

149320157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61871982-G-C

http://identifiers.org/hco/5/GRCh38#149320278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61871925-C-A

149320401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 61871815-T-G

149320476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61871740-G-A

149320503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61871716-C-T

149320509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61871706-T-C

149321129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61871515-G-A

149321305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61871361-A-G

149322456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870789-T-A

149322456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870789-T-G

149322490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870754-G-T

149322601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 61870683-A-G

149322614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 61870668-G-A

149322614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 61870668-G-T

149322642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 61870640-A-G

149329649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61870033-T-C

149329683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869999-T-C

149329825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869857-G-A

149329934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869746-A-G

149329940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869740-G-T

http://identifiers.org/hco/5/GRCh38#149329949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61869737-C-A

149329949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869737-C-G

149329949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869737-C-T

149330346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61869433-C-G

149331656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61869145-C-T

149332688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61868822-G-T

149332749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61868761-G-A

149332749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61868761-G-C

149332754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61868756-A-G

149332787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 61868723-C-T

http://identifiers.org/hco/5/GRCh38#149332895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61868618-C-A

149332895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868618-C-T

http://identifiers.org/hco/5/GRCh38#149332919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61868594-C-A

149332919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868594-C-T

149333804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868533-G-T

http://identifiers.org/hco/5/GRCh38#149333832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61868509-C-A

149333845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868487-G-A

149333907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868425-G-T

149333909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868423-A-G

149333939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868381-G-A

149333987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868331-T-C

149334293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868014-T-A

149334388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61867946-A-G

149335008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61867187-G-T

149335639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866856-C-T

149335675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866820-C-T

149335825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61866665-A-G

149336372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61866282-A-G

149340222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864209-G-A

149340222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864209-G-T

149340230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864202-G-T

149340283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864149-G-T

149340290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864142-C-T

http://identifiers.org/hco/5/GRCh38#149340421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61864033-C-A

149340421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864033-C-T

149340445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864009-G-A

149340445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61864009-G-C

http://identifiers.org/hco/5/GRCh38#149340545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61863908-A-C

149340545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863908-A-G

http://identifiers.org/hco/5/GRCh38#149340614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61863849-A-C

149340887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863597-T-C

149340887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863597-T-G

http://identifiers.org/hco/5/GRCh38#149341063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#61863425-C-A

149341063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863425-C-T

149341203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863272-A-T

149341255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863228-A-G

149341295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863188-T-C

149341331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863159-G-C

149341437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863069-T-C

149341494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863023-A-G

149341494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61863023-A-T

149341530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61862987-A-G

149341597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61862917-A-G

149341598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61862916-G-A

149341887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862541-A-G

149341955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862479-T-C

149342160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61862313-A-G

149342974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861601-A-G

149343077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861503-T-C

149343101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861482-C-T

149343142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861442-A-G

149343399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26714
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 61861233-A-G