136658856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470435-A-G

136658856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470435-A-T

136658903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470483-A-T

136658940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470538-G-A

136658940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470538-G-T

136658955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470570-A-G

136658976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470585-G-A

136658976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470585-G-T

http://identifiers.org/hco/9/GRCh38#136658997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26470604-C-A

136658997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470604-C-T

136658998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470605-C-T

http://identifiers.org/hco/9/GRCh38#136659026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26470631-C-A

http://identifiers.org/hco/9/GRCh38#136659032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26470637-C-A

136659032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470637-C-T

136659069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470667-G-T

http://identifiers.org/hco/9/GRCh38#136659103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26470718-C-A

http://identifiers.org/hco/9/GRCh38#136659199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26470808-C-A

136659209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470831-G-A

136659209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470831-G-C

136659209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470831-G-T

http://identifiers.org/hco/9/GRCh38#136659270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26470892-C-A

136659270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470892-C-T

136659318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470954-G-T

136659357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470996-G-A

136659357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470996-G-C

136659357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26470996-G-T

136659457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471094-T-C

136659564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471203-G-A

136659564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471203-G-T

136659575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471214-G-T

136659605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471238-C-T

http://identifiers.org/hco/9/GRCh38#136659689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26471314-C-A

136659794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471382-C-T

136660113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471637-G-A

136660242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471705-G-A

136660242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471705-G-T

http://identifiers.org/hco/9/GRCh38#136660314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26471775-C-A

136660324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 26471785-C-G

136660324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 26471785-C-T

136660327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26471788-C-G

136660327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26471788-C-T

136660408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471808-T-C

136660419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471821-C-T

136660457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26471857-T-C

http://identifiers.org/hco/9/GRCh38#136660489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26471885-C-A

136660489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471885-C-T

136660494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471890-G-T

136660516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471938-T-C

http://identifiers.org/hco/9/GRCh38#136660537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26471950-C-A

136660537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471950-C-T

136660547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471960-T-C

136660566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471976-G-A

136660566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26471976-G-T

136660832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472118-C-T

136660876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472146-T-C

136661080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472313-C-T

136661085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472317-C-G

136661085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472317-C-T

136661234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472376-G-T

136661249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472391-G-A

136661811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472832-G-A

136661857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26472859-G-A

136662295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26473281-G-T

136662447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26473436-G-A

136662629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26473588-C-T

136662926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26473888-T-C

136662948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26473911-G-A

136662948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26473911-G-T

136663081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 26474039-G-T

136663102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26474054-G-A

136663102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26474054-G-T

http://identifiers.org/hco/9/GRCh38#136663151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26474097-C-A

136663151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474097-C-T

http://identifiers.org/hco/9/GRCh38#136663155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26474101-C-A

136663155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474101-C-T

136663179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474122-G-A

136663179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474122-G-T

136663186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474129-G-A

136663186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474129-G-C

136663186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474129-G-T

136663316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474240-G-A

136663316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474240-G-T

136663425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474372-G-A

136663425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474372-G-T

136663493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474437-G-A

136663493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474437-G-T

136663546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474488-C-T

136663568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474508-A-G

136663578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474517-A-G

136663580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26474519-C-T

http://identifiers.org/hco/9/GRCh38#136663627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26474567-C-A

136663627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474567-C-T

http://identifiers.org/hco/9/GRCh38#136663726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26474661-C-A

136663726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474661-C-T

136663729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474664-T-C

http://identifiers.org/hco/9/GRCh38#136663730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26474665-C-A

136663820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474735-C-T

136663865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474772-G-A

136663929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474828-T-C

http://identifiers.org/hco/9/GRCh38#136663953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26474836-C-A

136663953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26474836-C-T

http://identifiers.org/hco/9/GRCh38#136664297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26475217-C-A

136664360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475280-G-A

136664360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475280-G-C

136664361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475281-G-A

136664441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475361-C-T

136664471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475391-T-C

136664501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475423-G-A

136664501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475423-G-T

136664681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475583-T-C

136664682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475584-C-T

http://identifiers.org/hco/9/GRCh38#136664713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26475615-C-A

136664713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26475615-C-T

136664736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26475638-A-G

http://identifiers.org/hco/9/GRCh38#136664793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26475695-C-A

http://identifiers.org/hco/9/GRCh38#136664801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26475704-C-A

136664858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475768-G-T

http://identifiers.org/hco/9/GRCh38#136664868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26475771-C-A

136664868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26475771-C-T

136665454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476306-G-T

http://identifiers.org/hco/9/GRCh38#136665487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26476337-C-A

136665640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476486-G-A

136665640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476486-G-T

136665712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476570-C-G

136665830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476706-C-T

136665885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476764-G-A

136665885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476764-G-T

136665917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26476791-T-C

136666243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477151-T-C

http://identifiers.org/hco/9/GRCh38#136666329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26477242-C-A

136666394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477309-A-G

136666498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477422-G-C

136666577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477494-G-T

136666590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477511-G-A

136666627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477542-G-C

136666684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477589-C-T

136666732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477642-C-T

136666867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477754-G-C

136666943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477824-T-A

136666943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26477824-T-C

136667226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478073-C-T

http://identifiers.org/hco/9/GRCh38#136667247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26478090-C-A

136667247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478090-C-T

136667252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478095-G-C

136667294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478141-C-T

136667383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478225-G-A

136667718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478564-G-A

136667799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478659-C-G

136667799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478659-C-T

136667904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478747-G-C

136667973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478819-T-C

136667985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478831-C-T

http://identifiers.org/hco/9/GRCh38#136668136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26478963-C-A

136668136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26478963-C-T

136668196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479015-G-A

136668196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479015-G-T

http://identifiers.org/hco/9/GRCh38#136668264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26479080-C-A

136668288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26479104-G-A

136668288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26479104-G-T

136668291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 26479107-C-T

136668295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26479111-C-G

http://identifiers.org/hco/9/GRCh38#136668447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26479264-C-A

136668447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479264-C-G

136668447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479264-C-T

http://identifiers.org/hco/9/GRCh38#136668498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26479289-C-A

136668498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479289-C-T

http://identifiers.org/hco/9/GRCh38#136668502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26479293-C-A

136668502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479293-C-T

136668623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26479408-C-T

136668768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479510-A-T

136669006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26479746-C-G

136669530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480330-G-A

136669530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480330-G-T

http://identifiers.org/hco/9/GRCh38#136669696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26480482-C-A

136669696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26480482-C-G

136669696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26480482-C-T

136669699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26480485-G-A

136669757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480542-G-A

136669757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480542-G-T

136669786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480560-G-A

http://identifiers.org/hco/9/GRCh38#136669790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26480564-C-A

136669792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480566-G-A

http://identifiers.org/hco/9/GRCh38#136669877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26480625-C-A

136669877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480625-C-T

136669951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26480706-T-C

136669951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26480706-T-G

http://identifiers.org/hco/9/GRCh38#136669963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26480718-C-A

136669963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26480718-C-G

136669963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26480718-C-T

136670074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480802-G-C

136670074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26480802-G-T

136670280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26481022-C-T

http://identifiers.org/hco/9/GRCh38#136670281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481023-A-C

136670281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26481023-A-G

http://identifiers.org/hco/9/GRCh38#136670303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481045-C-A

136670303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26481045-C-T

136670305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 26481047-C-G

http://identifiers.org/hco/9/GRCh38#136670452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481224-C-A

http://identifiers.org/hco/9/GRCh38#136670521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481300-A-C

136670521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481300-A-G

136670521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481300-A-T

http://identifiers.org/hco/9/GRCh38#136670564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481337-C-A

136670564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481337-C-T

http://identifiers.org/hco/9/GRCh38#136670771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481503-C-A

136670771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481503-C-T

http://identifiers.org/hco/9/GRCh38#136670773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481505-C-A

136670773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481505-C-G

136670773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481505-C-T

http://identifiers.org/hco/9/GRCh38#136670868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481584-C-A

136670868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481584-C-T

http://identifiers.org/hco/9/GRCh38#136670880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481604-A-C

http://identifiers.org/hco/9/GRCh38#136670931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481657-C-A

136670931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481657-C-T

136670937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481663-G-A

136670937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481663-G-T

136670946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26481672-G-A

136670946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26481672-G-T

136671398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481796-C-T

http://identifiers.org/hco/9/GRCh38#136671541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481892-C-A

http://identifiers.org/hco/9/GRCh38#136671605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481942-A-C

http://identifiers.org/hco/9/GRCh38#136671611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26481948-C-A

136671611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481948-C-T

136671615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481952-C-G

136671662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26481980-C-T

136671848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482079-C-T

http://identifiers.org/hco/9/GRCh38#136671868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26482094-C-A

136671868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482094-C-T

136672095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26482299-G-A

136672095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26482299-G-T

http://identifiers.org/hco/9/GRCh38#136672121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26482320-C-A

136672121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482320-C-T

136672144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482333-G-A

136672144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482333-G-C

136672144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482333-G-T

136672151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482336-T-C

136672169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482343-G-A

136672169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482343-G-C

http://identifiers.org/hco/9/GRCh38#136672243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#26482409-C-A

136672243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26482409-C-T

http://identifiers.org/hco/9/GRCh38#136672248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26482414-C-A

136672248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26482414-C-T

136672310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26482478-T-C

136672371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26482519-A-G

136672371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26482519-A-T

136672539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26482613-G-A

136672555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26482629-A-G

136672555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26482629-A-T

http://identifiers.org/hco/9/GRCh38#136672668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20594
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#26482684-A-C