161090424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61356987-T-C

161090572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61357140-C-T

161090665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61357234-C-T

161090998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61357550-T-G

161091122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61357674-T-C

161091234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61357814-T-A

161091630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61358125-A-G

161091646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61358139-A-G

161094802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61364165-T-G

161094898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61364280-G-A

161095009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61364390-A-T

161095219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61364590-G-A

161095327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61364699-C-T

161096244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369603-G-A

161096244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369603-G-T

161096253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369612-G-T

161096268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369628-G-C

161096429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369793-T-G

http://identifiers.org/hco/2/GRCh38#161096454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61369820-C-A

161096476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369842-G-A

161096476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61369842-G-T

161096567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 61369933-G-T

161097614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61370411-G-T

161097620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61370417-A-G

http://identifiers.org/hco/2/GRCh38#161097733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61370553-C-A

161097733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61370553-C-T

161099990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61372385-T-C

161100051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61372441-T-C

http://identifiers.org/hco/2/GRCh38#161100101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61372486-C-A

161100104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61372489-T-G

161100110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61372495-T-C

161100197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61373132-A-G

161100413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61373347-A-G

161100651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61373617-T-C

161100838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61373808-C-G

161100838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61373808-C-T

161101093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61374059-T-C

161101220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61374164-A-G

161101420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61374359-G-C

161101427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61374366-C-T

161101902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61374993-A-G

161101979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61375075-T-C

http://identifiers.org/hco/2/GRCh38#161102227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61375553-C-A

161102236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61375562-G-A

161102460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61375740-A-T

161102561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61375864-G-A

161102571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61375920-T-C

161102596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61375945-C-T

161103124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61376462-C-T

161103175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61376513-G-A

161103486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61376803-G-T

161103648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61377199-T-G

161103682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61377233-A-G

161104242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61377694-C-T

161104293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61377736-T-C

http://identifiers.org/hco/2/GRCh38#161104520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61377956-C-A

161104520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61377956-C-G

161104576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61378012-G-T

161105199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61378332-G-A

http://identifiers.org/hco/2/GRCh38#161105829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61378881-A-C

161106311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61379679-T-C

http://identifiers.org/hco/2/GRCh38#161106376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61379772-C-A

161106376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61379772-C-T

161106750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61380262-C-T

161106911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61380416-G-A

161107012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61380632-G-A

161107111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61380740-G-A

161107221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61380830-G-A

161107333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61380942-G-A

161107424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61381031-A-G

161108373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61382139-C-T

161108706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61382466-T-C

161109771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383223-A-G

161109790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383242-T-C

161109792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383244-C-G

161109792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383244-C-T

161109816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383268-C-T

161110243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61383892-T-C

http://identifiers.org/hco/2/GRCh38#161110248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61383898-A-C

161110498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384108-T-C

161110773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61384360-G-T

161111318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61385603-T-C

http://identifiers.org/hco/2/GRCh38#161111583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61385871-C-A

161111911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386202-T-C

161112630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386571-G-A

161112755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386742-G-T

161112836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386967-A-T

161112837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386968-T-A

161112837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386968-T-C

161112837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61386968-T-G

http://identifiers.org/hco/2/GRCh38#161113375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61387511-C-A

161113845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61387959-G-A

161113845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61387959-G-T

http://identifiers.org/hco/2/GRCh38#161113980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61388103-C-A

161114150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61388302-G-A

161116071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391114-A-G

161116089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391132-C-T

161116260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391307-T-C

161116391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391432-T-G

161116405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391446-G-T

161116682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391674-G-A

161116967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61391904-C-T

161117495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392336-G-A

161117517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392358-T-A

161117867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392697-A-G

161117903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392730-C-T

http://identifiers.org/hco/2/GRCh38#161117929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61392760-A-C

161117929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392760-A-T

161118027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392861-T-G

161118062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61392910-A-G

http://identifiers.org/hco/2/GRCh38#161118064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61392913-A-C

161118443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61393302-T-C

161118475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61393334-A-G

161118499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61393356-G-A

http://identifiers.org/hco/2/GRCh38#161119837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61395752-C-A

161120034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61395953-C-G

161120065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61395985-C-T

161120118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61396037-G-A

161120663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61396761-C-G

http://identifiers.org/hco/2/GRCh38#161120704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61396844-A-C

161120810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61396947-C-T

161120969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61397105-C-G

161122918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398094-C-T

161122926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398102-T-A

161122985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398165-A-G

http://identifiers.org/hco/2/GRCh38#161123000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61398180-A-C

161123000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398180-A-G

161123136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61398345-T-C

161123439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61399309-G-A

161123495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61399365-A-G

161123573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61399445-G-A

161123590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61399462-A-G

161123660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61399531-T-C

161128916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61401178-C-T

161129101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61401359-G-A

161129152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61401408-C-T

161129220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61401445-T-C

161129325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61401532-C-T

http://identifiers.org/hco/2/GRCh38#161129337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61401544-C-A

161129337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61401544-C-T

161129966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61402207-T-A

161129966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61402207-T-C

161130178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61402372-C-T

161130256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61402448-G-C

161130669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61403890-C-T

161131109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404034-G-T

161131148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404074-C-T

161131510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404427-A-G

161131510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404427-A-T

161131559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404478-G-A

http://identifiers.org/hco/2/GRCh38#161131726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61404644-C-A

161131726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404644-C-G

161131726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404644-C-T

161131832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404739-T-C

http://identifiers.org/hco/2/GRCh38#161131960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61404865-A-C

161131960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404865-A-G

161131981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61404885-G-A

161133374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405236-G-A

161133374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61405236-G-T

161135160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61407215-G-C

161135286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61407328-T-C

161135286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61407328-T-G

http://identifiers.org/hco/2/GRCh38#161135480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#61407528-C-A

161135630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61407686-T-G

http://identifiers.org/hco/2/GRCh38#161135756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61407802-A-C

161135820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61407868-T-C

http://identifiers.org/hco/2/GRCh38#161135956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61408005-C-A

161136207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61408213-A-T

http://identifiers.org/hco/2/GRCh38#161136476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61408448-A-C

161136804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61408779-C-T

http://identifiers.org/hco/2/GRCh38#161136931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#61408905-C-A

161136931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61408905-C-T

161137004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61408978-A-T

161137185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61409148-G-A

161137592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61409396-A-G

161137621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61409424-T-C

161138465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61409899-A-G

161138494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61409928-C-T

http://identifiers.org/hco/2/GRCh38#161138531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61409963-A-C

161138531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61409963-A-G

161138553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61409974-C-T

161138655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61410052-T-C

http://identifiers.org/hco/2/GRCh38#161138810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61410203-C-A

161138911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61410298-C-G

161139004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61410413-A-T

161139114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61410506-G-T

161139919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61411239-G-T

161139970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61411290-G-A

161140201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61411474-A-G

161140517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61411805-G-T

161140539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61411826-G-A

161140539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61411826-G-T

161156712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61418319-C-G

161156793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61418403-T-C

161157020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61418606-C-T

161157021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61418607-G-A

161157400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61418931-G-T

161157515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61419041-G-A

161157615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61419130-T-C

161158213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61419648-C-G

161158584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61421379-A-G

161158601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61421396-T-G

161159060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61421815-A-G

161159252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61421952-T-C

161159293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61421986-A-T

161159455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61422125-C-G

161159489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61422158-A-G

161159523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61422733-A-G

161159527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61422737-A-G

http://identifiers.org/hco/2/GRCh38#161159851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#61422993-C-A

161159971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61423099-G-C

http://identifiers.org/hco/2/GRCh38#161160087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#61423193-C-A

161160087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61423193-C-G

http://identifiers.org/hco/2/GRCh38#161160092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#61423198-A-C

161160206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61423299-T-C

http://identifiers.org/hco/2/GRCh38#161160219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#61423311-C-A

161160219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61423311-C-T

161160228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40575
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61423335-T-C