91261227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106988471-G-A

91261227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106988471-G-C

91261227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106988471-G-T

91261406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106988639-T-C

91261406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106988639-T-G

91261468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106988699-C-T

http://identifiers.org/hco/1/GRCh38#91261488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106988719-A-C

91261958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106989045-C-G

91261958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106989045-C-T

91262092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106989172-G-T

91262191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106989435-G-A

91262191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106989435-G-T

91262317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106989556-T-C

91262370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106989609-G-A

91262370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106989609-G-C

91262370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106989609-G-T

91262371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106989610-G-A

91262371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106989610-G-T

91262442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106990290-C-G

91262442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106990290-C-T

91262468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106990316-T-A

91262502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106990347-T-C

91262556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106990401-T-A

91262556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106990401-T-C

91262559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106990404-A-T

91262581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106990426-G-A

91262581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 106990426-G-T

91262717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106990604-T-C

91262969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106990976-T-G

91265261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106992577-T-C

91265498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106992791-G-T

91265652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106992930-T-C

91265749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993003-G-C

91265872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993125-G-A

91265872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993125-G-T

http://identifiers.org/hco/1/GRCh38#91265901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106993153-A-C

91265901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993153-A-G

91266078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106993312-T-C

http://identifiers.org/hco/1/GRCh38#91266092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106993326-A-C

91266149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993383-C-G

91266149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993383-C-T

91266165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106993399-T-C

http://identifiers.org/hco/1/GRCh38#91266250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106994041-C-A

91266250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106994041-C-T

91266588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106994164-T-C

http://identifiers.org/hco/1/GRCh38#91266680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106994238-A-C

91266682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106994240-T-A

91266700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106994258-G-A

91266958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106994491-T-G

91267189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106994716-G-A

http://identifiers.org/hco/1/GRCh38#91267661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106995401-C-A

91267661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995401-C-G

91267715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995500-G-A

91267715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995500-G-T

91267721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995506-A-G

91267728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995513-G-A

91267728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995513-G-T

91267848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106995636-C-G

91267849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106995637-A-G

91267889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995671-T-C

91267915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995697-A-G

91267920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995702-T-C

91268066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995848-C-G

91268066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995848-C-T

91268167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106995953-T-A

91269232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106996234-T-C

91269965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106996909-G-A

91269965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106996909-G-T

91270008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106996937-G-A

91270008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106996937-G-T

91270043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106996971-G-A

91270108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997034-G-A

91270126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997051-C-G

91270544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997432-G-T

http://identifiers.org/hco/1/GRCh38#91270582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#106997465-A-C

91270582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997465-A-G

91270804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997687-C-T

91270884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997759-G-A

91270986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106997891-T-A

91271194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106998096-T-C

91271218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106998119-G-A

91271221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106998122-T-C

91271313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106998215-C-G

91271392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106998317-T-A

91271506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106998443-A-G

91272044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999098-G-T

91272295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999336-C-T

91272301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999342-A-G

91272465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999525-T-C

91272570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999600-G-C

91272578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999608-T-C

91272602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106999632-G-A

91273416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107000702-T-G

91273556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107000835-C-G

91273571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107000850-G-T

91273640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107000918-A-G

91273640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107000918-A-T

91273721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107000993-G-T

91273755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107001027-G-A

91273755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107001027-G-T

91273798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107001070-A-G

91273862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107001128-T-A

91273862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107001128-T-C

91273921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107001189-C-T

http://identifiers.org/hco/1/GRCh38#91274321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107002237-C-A

91274321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002237-C-T

91274570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002445-G-A

91274586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002461-T-G

91274637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002515-G-A

91274637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002515-G-T

91274662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002540-A-G

91274663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002541-G-T

http://identifiers.org/hco/1/GRCh38#91274801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107002678-C-A

91274812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107002689-A-G

91274814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107002691-T-A

91274814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107002691-T-C

http://identifiers.org/hco/1/GRCh38#91274873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107002745-C-A

91274873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107002745-C-T

http://identifiers.org/hco/1/GRCh38#91274892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107002764-C-A

91275599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107003576-G-A

91275749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107003708-T-G

91276144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004242-G-A

91276144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004242-G-T

91276212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004297-C-G

91276587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004712-T-G

91276604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004729-G-A

91276604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004729-G-C

91276604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107004729-G-T

91276704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107004819-G-A

91276704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107004819-G-C

91276704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107004819-G-T

91276728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107004843-G-A

91276728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107004843-G-T

91276890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005167-A-T

http://identifiers.org/hco/1/GRCh38#91276926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107005207-C-A

91276926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005207-C-T

91276938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005219-T-C

http://identifiers.org/hco/1/GRCh38#91277098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107005518-C-A

91277098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005518-C-G

91277098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005518-C-T

91277153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005571-T-A

91277203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005617-T-C

http://identifiers.org/hco/1/GRCh38#91277204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107005618-C-A

http://identifiers.org/hco/1/GRCh38#91277223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107005631-A-C

91277223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005631-A-G

91277344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107005645-C-T

91278263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107006282-T-C

91278533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107006512-A-G

91282421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107008034-C-G

http://identifiers.org/hco/1/GRCh38#91282510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107008118-A-C

91282510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107008118-A-G

91282867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107008430-T-C

91283039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107008621-G-T

91310202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019104-A-G

91313163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019449-T-C

91313266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019567-G-A

91313266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019567-G-T

91313287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019585-G-A

91313287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019585-G-T

91313357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019655-G-A

91313357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019655-G-T

91313412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019710-A-G

91313429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019727-A-G

91313451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019749-G-A

91313455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019753-T-A

91313455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107019753-T-G

http://identifiers.org/hco/1/GRCh38#91313517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107019815-C-A

91313517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019815-C-T

http://identifiers.org/hco/1/GRCh38#91313581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107019878-C-A

91313581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019878-C-G

91313581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019878-C-T

91313644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107019937-T-A

91313892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020123-G-A

91313892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020123-G-C

91313892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020123-G-T

91313940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020170-T-C

http://identifiers.org/hco/1/GRCh38#91314090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107020336-C-A

91314131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020377-T-C

91314270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020487-T-C

91314876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107020915-G-C

91315043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107021051-G-A

91315096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107021112-G-A

91315255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107021246-G-C

http://identifiers.org/hco/1/GRCh38#91315302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107021282-A-C

91315302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107021282-A-G

91315996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107021983-A-G

http://identifiers.org/hco/1/GRCh38#91316019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107022005-C-A

91316023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107022009-T-C

91316096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107022064-T-G

91316135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107022103-A-G

91316272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107022243-G-T

91316482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107022800-G-A

91316482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107022800-G-T

91316560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107022872-T-A

91317514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107024151-T-A

http://identifiers.org/hco/1/GRCh38#91317570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107024207-A-C

91317589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107024226-T-C

91317974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107024584-G-A

91319068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107026448-C-G

91319097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107026476-G-T

http://identifiers.org/hco/1/GRCh38#91319144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107026523-C-A

91319144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107026523-C-G

91319432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107026807-A-G

91319444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107026832-G-T

91319487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107026868-C-T

91322982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107028197-T-C

91323002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107028217-A-G

91323019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028232-A-G

91323065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028273-T-A

91323080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028288-G-A

91323080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028288-G-T

http://identifiers.org/hco/1/GRCh38#91323105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107028313-C-A

91323105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107028313-C-T

91323241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028449-T-C

91323269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028477-T-C

91323269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028477-T-G

91323647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028802-T-C

91323724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028830-G-A

91323802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028894-T-C

91323866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107028956-C-G

91324025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107029091-T-C

91324530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107029529-A-G

91324530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107029529-A-T

http://identifiers.org/hco/1/GRCh38#91324571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107029566-C-A

91324571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107029566-C-T

91324681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107029665-T-C

91324682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107029666-G-A

91324682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107029666-G-T

91333791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107029855-T-C

91333815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107029880-G-T

91334154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107030191-A-G

91334168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107030202-T-C

91335500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107031129-T-C

91343403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107034349-A-G

91343405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107034351-T-C

91343408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107034354-A-G

91343408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107034354-A-T

http://identifiers.org/hco/1/GRCh38#91343548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107034495-A-C

91343871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107034791-A-T

91344049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035530-C-T

91344086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035566-A-G

91344105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035584-C-T

http://identifiers.org/hco/1/GRCh38#91344130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107035610-C-A

91344130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035610-C-T

91344156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035671-C-T

91344176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035693-G-C

91344431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107035927-C-T

91344537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107036035-A-G

91344564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107036065-C-T

91344656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107036154-G-A

91344656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107036154-G-T

91347050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037410-A-G

http://identifiers.org/hco/1/GRCh38#91347068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107037421-C-A

91347263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037617-A-G

91347305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037644-T-G

http://identifiers.org/hco/1/GRCh38#91347317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107037654-C-A

91347317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037654-C-G

91347317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037654-C-T

91347391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037726-T-A

91347497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037850-A-G

http://identifiers.org/hco/1/GRCh38#91347592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107037930-C-A

http://identifiers.org/hco/1/GRCh38#91347606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107037944-C-A

91347606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107037944-C-G

91347958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107038204-T-C

91348080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107038372-G-T

91348248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107038512-G-C

91348300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107038555-G-A

91348300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107038555-G-C

91350644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040462-T-C

91350698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040522-C-T

91350793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107040619-T-C

91350823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107040649-A-G

91350823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 107040649-A-T

91350931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040758-T-A

91350931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040758-T-C

91350978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040799-G-A

91350978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040799-G-T

91351073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040883-G-A

91351089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040908-T-C

http://identifiers.org/hco/1/GRCh38#91351112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107040925-A-C

91351112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107040925-A-G

91351289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041081-T-A

91351459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041238-T-C

91351459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041238-T-G

http://identifiers.org/hco/1/GRCh38#91351460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107041239-C-A

91351460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041239-C-G

91351460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041239-C-T

http://identifiers.org/hco/1/GRCh38#91351474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107041252-C-A

91351474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041252-C-T

91351520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041291-T-C

http://identifiers.org/hco/1/GRCh38#91351533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107041304-C-A

91351533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041304-C-T

91351587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 107041354-G-T

91351635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107041402-A-G

91351745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041487-G-C

91351745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041487-G-T

http://identifiers.org/hco/1/GRCh38#91351854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107041565-A-C

91351854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107041565-A-T

91352090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107042551-A-G

91352134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107042581-G-A

91352253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107042782-T-A

91352625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107043181-C-G

91352626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107043182-T-C

http://identifiers.org/hco/1/GRCh38#91352691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107043240-C-A

91352691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043240-C-T

91352718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043269-T-A

91352772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043323-G-A

91352772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043323-G-T

91352791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043342-C-T

91352900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043447-G-T

91352916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107043461-T-C

91353614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107045215-T-A

91375207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107045990-T-A

91375207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107045990-T-C

91375223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046006-A-T

91375321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046102-A-G

http://identifiers.org/hco/1/GRCh38#91375475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107046241-A-C

91375475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046241-A-T

91375548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107046316-A-T

http://identifiers.org/hco/1/GRCh38#91375855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107046631-C-A

91375855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046631-C-T

http://identifiers.org/hco/1/GRCh38#91375863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107046639-C-A

91375872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046648-T-C

91375984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046747-T-C

91376159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107046917-T-C

91377863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107049053-G-T

91378098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107049641-G-C

http://identifiers.org/hco/1/GRCh38#91378205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107049748-A-C

http://identifiers.org/hco/1/GRCh38#91378214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107049757-C-A

91378214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107049757-C-T

91378326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107049863-T-A

91378326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107049863-T-C

http://identifiers.org/hco/1/GRCh38#91378350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107049885-C-A

91378350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107049885-C-T

91378355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107049888-T-A

91378355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107049888-T-C

91378495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050021-A-G

91378501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050027-A-G

91378510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050036-T-C

91378828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050570-A-T

91378829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050571-C-T

91378907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050648-G-T

91378947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050683-G-A

91378947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107050683-G-T

91379304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107051023-T-C

91379313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107051032-A-G

91379335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107051048-T-G

http://identifiers.org/hco/1/GRCh38#91379639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107051108-A-C

91379642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107051111-G-C

91379776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107051238-A-G

91379868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107051327-T-C

91379873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107051335-G-A

91380087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052075-T-C

91380087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052075-T-G

91380153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107052141-T-C

91380278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052262-T-C

http://identifiers.org/hco/1/GRCh38#91380353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107052335-C-A

91380374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052354-A-T

91380380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052360-G-A

91380380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052360-G-T

http://identifiers.org/hco/1/GRCh38#91380771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107052532-A-C

91380771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052532-A-G

91380819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052555-G-A

91380819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052555-G-T

91380954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107052654-T-C

91380967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107052667-C-T

http://identifiers.org/hco/1/GRCh38#91380980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107052680-C-A

91380980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107052680-C-T

91381068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052767-T-A

91381068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052767-T-C

http://identifiers.org/hco/1/GRCh38#91381104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107052939-C-A

91381104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107052939-C-T

http://identifiers.org/hco/1/GRCh38#91381194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107053091-A-C

91381877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107054038-G-C

91382033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107054197-T-C

91382731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107055519-T-C

91382850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107055642-T-G

91382925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107055726-G-T

91382926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107055727-T-G

91383019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107056617-C-T

91385129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107058884-T-C

http://identifiers.org/hco/1/GRCh38#91385233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107058984-C-A

91385233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 107058984-C-T

91385237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107058988-G-A

91385237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107058988-G-T

91385413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059106-C-G

http://identifiers.org/hco/1/GRCh38#91385518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107059198-C-A

91385518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059198-C-T

91385526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059206-T-A

91385526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059206-T-C

91385541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059221-A-T

91385665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107059360-C-G

91385741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107059436-T-C

91385860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059551-A-G

91385893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059575-A-T

91385899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059581-T-C

http://identifiers.org/hco/1/GRCh38#91385902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107059584-C-A

91386188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059810-T-C

91386228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059862-G-A

http://identifiers.org/hco/1/GRCh38#91386235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107059869-C-A

91386236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107059870-A-T

91386578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107060186-C-T

91394010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107065114-A-G

91394050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107065153-A-G

http://identifiers.org/hco/1/GRCh38#91394296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107065393-A-C

91394296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107065393-A-G

91394300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107065397-G-C

91395790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107066198-C-T

http://identifiers.org/hco/1/GRCh38#91396246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107066198-C-A

91396296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107066246-A-G

91397517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107067113-G-A

91397828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107067240-C-T

91397862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107067274-C-T

91398016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107067419-T-C

91398077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107067479-G-T

91398314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107067701-T-C

91399014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107068390-A-G

91399114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107068995-C-T

91399131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107069011-G-T

91399234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107069115-T-C

91399352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107069215-C-T

91399372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107069240-C-G

91399596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107069460-T-C

91399739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107069602-C-G

http://identifiers.org/hco/1/GRCh38#91399823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107069659-C-A

91400596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070321-C-T

http://identifiers.org/hco/1/GRCh38#91400630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107070346-C-A

91400630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070346-C-T

91400643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070359-G-A

91400684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070385-A-G

http://identifiers.org/hco/1/GRCh38#91400705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107070412-A-C

http://identifiers.org/hco/1/GRCh38#91401092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107070759-C-A

91401129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070794-T-G

91401204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070879-A-T

http://identifiers.org/hco/1/GRCh38#91401222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107070897-C-A

91401225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070900-C-T

http://identifiers.org/hco/1/GRCh38#91401247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107070922-C-A

http://identifiers.org/hco/1/GRCh38#91401259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107070931-C-A

91401259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070931-C-G

91401259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107070931-C-T

91401367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071027-C-G

91401996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071157-A-T

91402076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071234-T-C

91402138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071296-G-C

91402275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071430-C-T

http://identifiers.org/hco/1/GRCh38#91402307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107071461-A-C

91402318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071471-T-C

91402320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071473-T-G

91402408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071642-T-C

http://identifiers.org/hco/1/GRCh38#91402432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107071856-C-A

91402482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071911-C-T

91402544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107071971-A-G

91402593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107072023-C-G

91402608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107072040-A-G

http://identifiers.org/hco/1/GRCh38#91402747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107072359-C-A

91403109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107072684-T-G

91403141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107072711-A-G

91403476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107072990-T-A

91403476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107072990-T-C

91403625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073257-C-T

http://identifiers.org/hco/1/GRCh38#91403687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107073318-A-C

91403780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073367-A-G

http://identifiers.org/hco/1/GRCh38#91403895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107073449-C-A

91404133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073568-C-T

91404155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073590-C-T

91404356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073767-A-G

91404364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073778-C-G

http://identifiers.org/hco/1/GRCh38#91404367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107073781-C-A

91404367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107073781-C-G

91404467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107073850-G-C

http://identifiers.org/hco/1/GRCh38#91404493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107073881-C-A

91404496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107073884-C-T

91404500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107073888-A-G

91404680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107074019-G-A

91404680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107074019-G-C

91404749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107074064-G-A

91404752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107074067-C-T

91404757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107074075-G-A

http://identifiers.org/hco/1/GRCh38#91404759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107074077-C-A

91404772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107074090-G-T

91404806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107074122-G-A

91404806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 107074122-G-C

91404818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107074134-G-A

91404818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107074134-G-C

91404818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107074134-G-T

91404825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107074142-C-G

http://identifiers.org/hco/1/GRCh38#91404829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#107074146-C-A

91404894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20193
most severe consequence: intron variant
orthologous variants: 107074211-G-A