67518410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106321780-T-C

http://identifiers.org/hco/16/GRCh38#67518479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106321851-C-A

67518479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106321851-C-T

http://identifiers.org/hco/16/GRCh38#67518600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106321969-C-A

67518600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106321969-C-T

67518730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106322099-G-A

67518864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106322205-G-A

67519766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106322733-C-T

67521053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106322968-G-A

67521182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106323099-G-T

67521660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106323565-A-G

67521680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106323585-G-A

67521891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106323803-A-G

67523898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325481-T-G

67523936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325512-C-T

67524102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325605-T-C

67524122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325623-T-C

http://identifiers.org/hco/16/GRCh38#67524138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106325641-A-C

67524459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326345-T-C

67524503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326387-C-G

67524595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326451-A-G

67524797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326616-C-T

67524821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326637-C-T

67525153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326980-A-G

67525447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327790-T-G

67525527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327863-G-A

67525946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106328222-C-T

67526069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106328334-C-T

67526800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106330320-A-G

67527611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106330623-T-C

67527798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106330846-C-T

67527921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106330949-C-T

67528237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106331253-G-T

http://identifiers.org/hco/16/GRCh38#67528265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331294-C-A

67528265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106331294-C-T

http://identifiers.org/hco/16/GRCh38#67528321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331354-C-A

67528321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106331354-C-T

67528326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106331359-A-G

67528342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106331374-G-A

http://identifiers.org/hco/16/GRCh38#67528347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331379-C-A

67528347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106331379-C-T

http://identifiers.org/hco/16/GRCh38#67528350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331382-C-A

http://identifiers.org/hco/16/GRCh38#67528420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331458-C-A

67528420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106331458-C-T

67528440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106331491-G-T

http://identifiers.org/hco/16/GRCh38#67528650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331722-C-A

67528650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106331722-C-T

http://identifiers.org/hco/16/GRCh38#67528731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331805-A-C

67528731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106331805-A-G

67528850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106331918-G-A

67528850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106331918-G-T

http://identifiers.org/hco/16/GRCh38#67528851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106331919-C-A

67528851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106331919-C-G

67528851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106331919-C-T

67528872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106331940-A-G

67528897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106331965-G-A

67528897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106331965-G-C

67528897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106331965-G-T

67528967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332033-G-A

67528967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332033-G-C

67528967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332033-G-T

67528987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332054-G-A

67528987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332054-G-C

67528987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332054-G-T

http://identifiers.org/hco/16/GRCh38#67529060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106332127-C-A

67529284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332352-G-A

67529284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332352-G-C

67529284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332352-G-T

67529420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332492-T-C

67529559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332630-G-A

67529559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332630-G-C

67529559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332630-G-T

http://identifiers.org/hco/16/GRCh38#67529615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106332687-C-A

67529615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332687-C-T

http://identifiers.org/hco/16/GRCh38#67529633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106332705-C-A

67529647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332719-G-A

67529647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332719-G-T

67529681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106332753-G-T

http://identifiers.org/hco/16/GRCh38#67530026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106333044-C-A

67530026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106333044-C-T

http://identifiers.org/hco/16/GRCh38#67530048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106333066-C-A

67530048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106333066-C-T

67530132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106333139-G-T

http://identifiers.org/hco/16/GRCh38#67530228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106333240-C-A

67530228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106333240-C-T

67530825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106333831-G-A

67530993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106334007-A-G

67531085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106334119-G-A

67531403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106334584-G-A

67531403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106334584-G-T

67531457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106334634-G-T

67531490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106334678-G-T

67531553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106334775-A-G

http://identifiers.org/hco/16/GRCh38#67531565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106334791-C-A

67531693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335017-G-C

67535233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106338466-G-A

67535387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106338616-G-A

67535550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106338775-G-A

67535716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106338931-G-A

67535836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339054-T-C

67536606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339224-G-T

67537364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339742-C-G

67537364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339742-C-T

67537368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339746-T-A

67537368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339746-T-C

67537540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106339948-G-A

67537540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106339948-G-T

http://identifiers.org/hco/16/GRCh38#67537577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106339985-C-A

67537577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106339985-C-G

67537577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106339985-C-T

67537674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340083-G-A

http://identifiers.org/hco/16/GRCh38#67537705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106340121-C-A

67537705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340121-C-T

67537748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340162-C-G

67537748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340162-C-T

67537838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106340438-T-A

67537998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340598-G-A

67537998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340598-G-C

67537998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340598-G-T

http://identifiers.org/hco/16/GRCh38#67538011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106340611-C-A

67538011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340611-C-G

http://identifiers.org/hco/16/GRCh38#67538052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106340656-C-A

67538052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340656-C-G

67538052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340656-C-T

http://identifiers.org/hco/16/GRCh38#67538212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#106340817-C-A

67538212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106340817-C-G

67538212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106340817-C-T

67538272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106340876-C-T

67538569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106341172-T-C

67538643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106341244-C-T

67538680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106341281-C-T

67538689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106341290-G-A

67539091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106341673-G-A

67539288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106341858-G-T

http://identifiers.org/hco/16/GRCh38#67539497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106341975-A-C

http://identifiers.org/hco/16/GRCh38#67539499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106341977-C-A

67539887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106342217-C-T

67540062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106342354-C-T

67540109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106342401-C-T

67540158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106342450-C-G

67540158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106342450-C-T

67540182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106342474-C-T

http://identifiers.org/hco/16/GRCh38#67540286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106342598-C-A

67540286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106342598-C-G

67540286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106342598-C-T

http://identifiers.org/hco/16/GRCh38#67540381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106342692-C-A

67540381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106342692-C-T

http://identifiers.org/hco/16/GRCh38#67540714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106343029-C-A

67540714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106343029-C-T

http://identifiers.org/hco/16/GRCh38#67541296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106343401-C-A

67541296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106343401-C-G

http://identifiers.org/hco/16/GRCh38#67541301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106343406-C-A

http://identifiers.org/hco/16/GRCh38#67541394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106343474-C-A

67541394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106343474-C-T

67541412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106343492-A-G

67541616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343697-G-C

67541618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343699-C-G

67541689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106343770-T-A

67541689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106343770-T-G

67541710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106343791-A-G

67541830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343912-T-C

67541848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343929-G-A

67541893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106343974-G-A

67541923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106344004-T-C

67541950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106344031-A-T

67542064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106344142-C-T

67542253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106344328-G-A

67542255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106344330-A-G

67542270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106344345-C-G

67542271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106344346-T-A

67542414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344489-G-A

67542414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344489-G-T

67542627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344699-G-A

67542627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344699-G-T

http://identifiers.org/hco/16/GRCh38#67542639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106344711-C-A

67542639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344711-C-T

http://identifiers.org/hco/16/GRCh38#67542660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106344732-C-A

67542662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344734-C-G

67542662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106344734-C-T

67542688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106344760-T-C

http://identifiers.org/hco/16/GRCh38#67542764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106344854-C-A

67542949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106345042-C-G

67542949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106345042-C-T

67542974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106345067-G-A

67542974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106345067-G-C

67542974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106345067-G-T

67543078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106345171-G-A

67543078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106345171-G-C

67543078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106345171-G-T

67543163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106345256-G-A

67543627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106345735-T-G

http://identifiers.org/hco/16/GRCh38#67543629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106345737-C-A

67543629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106345737-C-T

67543740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106345853-G-A

67543740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106345853-G-C

67543740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106345853-G-T

http://identifiers.org/hco/16/GRCh38#67543827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106345941-C-A

67543827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106345941-C-T

67543831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106345945-G-A

67543831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106345945-G-T

67543864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106345979-T-C

67544119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346243-A-G

http://identifiers.org/hco/16/GRCh38#67544181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346301-C-A

http://identifiers.org/hco/16/GRCh38#67544214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346330-C-A

67544214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346330-C-T

67544254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346370-T-C

67544254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346370-T-G

67544280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346400-G-A

67544280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346400-G-T

http://identifiers.org/hco/16/GRCh38#67544377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346498-A-C

67544378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106346499-G-T

67544443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346563-G-T

67544456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346576-C-G

67544481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346595-G-A

http://identifiers.org/hco/16/GRCh38#67544488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346602-C-A

67544488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346602-C-T

http://identifiers.org/hco/16/GRCh38#67544509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346622-C-A

67544509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346622-C-T

67544587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346697-A-G

http://identifiers.org/hco/16/GRCh38#67544593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346703-C-A

67544593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106346703-C-T

http://identifiers.org/hco/16/GRCh38#67544746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106346862-C-A

67544746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106346862-C-G

67544746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106346862-C-T

67544924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347016-T-A

67544924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347016-T-G

http://identifiers.org/hco/16/GRCh38#67544945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106347036-C-A

67544945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347036-C-T

67544947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347038-C-T

67544981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106347072-T-G

67545129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347236-G-T

http://identifiers.org/hco/16/GRCh38#67545230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106347338-A-C

67545230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347338-A-G

67545250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347365-A-G

67545250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347365-A-T

http://identifiers.org/hco/16/GRCh38#67545253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106347366-A-C

67545253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347366-A-G

67545264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106347380-G-A

67545407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106347513-G-A

67545450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106347556-C-G

67545572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106347684-G-A

67545581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106347707-A-G

67545928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106348004-T-G

67545944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106348021-C-T

67545946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106348023-C-T

http://identifiers.org/hco/16/GRCh38#67546044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106348122-C-A

67546044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106348122-C-G

67546106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106348168-C-T

67546356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106348427-C-G

67546539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348607-G-A

67546539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348607-G-T

67546581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348648-G-T

67546705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348776-G-A

http://identifiers.org/hco/16/GRCh38#67546709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#106348779-C-A

67546728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348798-G-A

67546728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348798-G-T

67546783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25836
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106348860-C-T