10946644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148761351-T-C

http://identifiers.org/hco/1/GRCh38#10946664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148761331-C-A

10946664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148761331-C-T

10946843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761176-A-T

10946860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761165-G-A

10947100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761099-G-A

10947462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148760912-C-G

10947517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148760864-T-C

10947528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761366-A-G

http://identifiers.org/hco/1/GRCh38#10947535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148761373-C-A

10947535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761373-C-T

10947542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761381-G-A

10947542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761381-G-T

http://identifiers.org/hco/1/GRCh38#10947543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148761382-C-A

10947543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 148761382-C-T

10947775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760688-G-A

10947775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760688-G-C

10947775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760688-G-T

10947794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760677-A-G

10947809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760662-C-G

10947809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760662-C-T

10947816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760655-G-A

10947816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760655-G-T

10948025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760476-T-A

10948025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760476-T-C

10948043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760458-G-A

10948071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760430-G-A

10948071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760430-G-C

10948081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760420-G-T

10948083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760418-T-A

10948098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760400-G-A

10948098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760400-G-T

10948103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760395-T-C

10948103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760395-T-G

10948172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148760344-G-A

10948497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148760013-A-G

10948696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148759814-G-A

10948696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148759814-G-C

http://identifiers.org/hco/1/GRCh38#10948894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759624-C-A

http://identifiers.org/hco/1/GRCh38#10948895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759623-A-C

10948895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759623-A-G

http://identifiers.org/hco/1/GRCh38#10948952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759574-C-A

10948952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759574-C-T

10948953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759573-G-A

10948953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759573-G-T

10949029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759555-G-A

10949029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759555-G-T

http://identifiers.org/hco/1/GRCh38#10949194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759547-A-C

10949194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759547-A-G

10949194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759547-A-T

10949264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759538-T-A

10949264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759538-T-C

http://identifiers.org/hco/1/GRCh38#10949271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759531-C-A

10949301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759502-T-A

10949437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759374-G-A

10949437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759374-G-T

http://identifiers.org/hco/1/GRCh38#10949455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759356-A-C

10949455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759356-A-G

10949464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759347-A-G

10949464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759347-A-T

http://identifiers.org/hco/1/GRCh38#10949478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759333-A-C

10949541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 148759255-G-T

10949564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148759232-T-C

10949565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148759231-T-A

10949588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 148759205-G-T

10949686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148759116-G-A

10949692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148759110-C-G

10949692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 148759110-C-T

http://identifiers.org/hco/1/GRCh38#10949700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148759102-A-C

10949700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 148759102-A-G

10949700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_donor_variant
orthologous variants: 148759102-A-T

10949758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense variant
orthologous variants: 148759044-G-A

10949758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense variant
orthologous variants: 148759044-G-T

10949799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense variant
orthologous variants: 148759003-G-A

10949799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: stop gained
orthologous variants: 148759003-G-T

10949856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148758945-G-A

10949856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148758945-G-T

10949870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148758931-A-G

http://identifiers.org/hco/1/GRCh38#10949887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148758914-C-A

10949904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148758895-T-A

10950324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148758494-C-G

10951894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148756473-G-A

10952021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148756374-A-T

10953347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148755379-T-G

10953568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148755154-C-T

http://identifiers.org/hco/1/GRCh38#10953922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148753527-C-A

10953922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148753527-C-T

http://identifiers.org/hco/1/GRCh38#10953945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148753504-C-A

10953945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148753504-C-T

10953959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148753492-G-T

10953979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148753472-C-T

10953990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148753461-C-T

10954945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148753114-C-T

10954993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: synonymous variant
orthologous variants: 148753071-G-A

10954993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: synonymous variant
orthologous variants: 148753071-G-T

10955007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense variant
orthologous variants: 148753057-C-T

10955147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense variant
orthologous variants: 148752917-G-T

http://identifiers.org/hco/1/GRCh38#10955333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148752783-C-A

10955333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148752783-C-T

10955384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148752747-G-C

http://identifiers.org/hco/1/GRCh38#10957043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#148751871-A-C

10957043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, missense_variant
orthologous variants: 148751871-A-G

http://identifiers.org/hco/1/GRCh38#10957149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148751772-C-A

10957149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751772-C-T

http://identifiers.org/hco/1/GRCh38#10957184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148751737-C-A

10957184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751737-C-T

10957259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751659-G-A

10957445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751473-G-T

10957465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751453-G-A

10957465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751453-G-T

10957482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751436-G-A

10957482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751436-G-T

10957538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751381-G-T

10957737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: missense variant
orthologous variants: 148751177-G-A

10957853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148751004-C-T

10957921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750848-C-T

10957926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750843-G-A

10957926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750843-G-T

10958006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750787-A-G

10958017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750776-A-G

10958044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750750-G-A

10958046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750748-C-T

10958130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750661-G-A

10958208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750589-G-C

10958216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750580-A-G

10958279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750538-G-A

10958300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148750517-C-T

10958349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148749180-G-A

http://identifiers.org/hco/1/GRCh38#10958365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148749164-A-C

10958373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148749156-A-G

10958497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148749052-T-G

10958534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148749012-A-T

10958538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148749008-G-C

10958564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748993-A-T

http://identifiers.org/hco/1/GRCh38#10958589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148748968-C-A

10958589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748968-C-T

10958607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748945-G-A

10958607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748945-G-T

10958689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748888-T-G

10958766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748826-G-A

10958766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748826-G-C

http://identifiers.org/hco/1/GRCh38#10958789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148748806-C-A

10958789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748806-C-T

http://identifiers.org/hco/1/GRCh38#10958835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148748776-C-A

10958835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748776-C-G

10958835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748776-C-T

10958862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748749-G-A

10958862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748749-G-T

10959246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748400-C-T

10959373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748214-G-A

10959375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148748212-C-T

10959601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148747949-C-G

10959624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148747925-A-G

10959773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148747793-C-T

http://identifiers.org/hco/1/GRCh38#10960564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148747333-A-C

10960564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148747333-A-G

10960620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148747277-C-T

10960623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148747274-G-A

10961038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148746870-A-T

10961065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148746859-C-T

10961134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148746799-T-C

10961166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148746781-A-G

10961169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148746778-A-G

10961577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148746443-G-T

10961615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148746404-C-T

10962172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148745942-G-A

10962172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148745942-G-C

http://identifiers.org/hco/1/GRCh38#10963495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148744936-C-A

10963495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148744936-C-T

10963574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148744899-C-T

10964034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743626-G-A

10964098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743564-G-A

10964105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743547-C-G

10964106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743546-C-T

10964306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743346-G-A

10964306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743346-G-T

10964396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743266-G-A

10964396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743266-G-T

10964537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148743119-A-G

10966410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 148742559-T-C

10966489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 148742485-T-C

10966489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 148742485-T-G

10966507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148742467-G-A

10968180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148741739-T-A

10969264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148740544-G-A

10969662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148739710-G-A

10969799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148739587-G-A

10975309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148736245-G-A

10975349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148736197-G-A

http://identifiers.org/hco/1/GRCh38#10975411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148736156-A-C

10975411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148736156-A-G

10975519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148736058-G-C

10975520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148736057-T-G

10975990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148735849-T-A

10975990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148735849-T-C

10976092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735760-T-C

10976095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735757-G-T

10976107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148735745-G-A

10976141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148735712-G-T

10976202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: synonymous_variant, undefined
orthologous variants: 148735651-G-A

http://identifiers.org/hco/1/GRCh38#10976307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148735544-C-A

10976307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735544-C-T

http://identifiers.org/hco/1/GRCh38#10976328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148735518-A-C

10976328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735518-A-T

10976329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735517-T-A

10976329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735517-T-C

10976329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735517-T-G

http://identifiers.org/hco/1/GRCh38#10976337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148735509-C-A

10976337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735509-C-T

10976385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735462-G-T

10976500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735342-T-C

10976659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735190-T-C

10976659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735190-T-G

10976676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735173-T-A

10976813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148735031-G-A

10980424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148728811-G-A

10980630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron_variant, undefined
orthologous variants: 148728628-C-T

10980779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148728489-C-T

10980950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148728326-C-T

10981782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148728119-A-T

10981787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148728114-T-A

10981787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148728114-T-C

10981823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148728077-C-T

http://identifiers.org/hco/1/GRCh38#10981881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148727998-C-A

10981956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148727923-T-C

10981956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: intron variant
orthologous variants: 148727923-T-G

10982047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26730
most severe consequence: 5 prime UTR variant
orthologous variants: 148727804-C-T