121035626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 3 prime UTR variant
orthologous variants: 65682055-G-A

http://identifiers.org/hco/4/GRCh38#121035948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65681720-A-C

121036110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 3 prime UTR variant
orthologous variants: 65681560-A-G

121036247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 3 prime UTR variant
orthologous variants: 65681438-T-A

121036512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65681179-C-G

121036512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65681179-C-T

121036526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65681165-T-A

121036526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65681165-T-C

121036754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65680937-T-C

121036754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65680937-T-G

121037009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense variant
orthologous variants: 65680682-C-T

121037417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65680274-G-C

121037534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 65680157-T-C

http://identifiers.org/hco/4/GRCh38#121037817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65679833-C-A

http://identifiers.org/hco/4/GRCh38#121037841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65679786-A-C

121037841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679786-A-G

121037841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679786-A-T

121037957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65679587-C-T

121037990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65679551-A-G

121038023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65679518-A-G

http://identifiers.org/hco/4/GRCh38#121038034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65679507-A-C

121039657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678775-A-T

121039792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678678-T-A

121039792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678678-T-C

http://identifiers.org/hco/4/GRCh38#121039808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65678662-C-A

121039808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678662-C-T

http://identifiers.org/hco/4/GRCh38#121039809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65678661-C-A

121039809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678661-C-T

121039824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678649-T-G

121040056-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: undefined
orthologous variants: 65678423-T-A

121040124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678365-A-G

121040124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678365-A-T

http://identifiers.org/hco/4/GRCh38#121040125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65678364-A-C

121040125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678364-A-G

121040443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678128-C-T

121040445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678126-C-G

121040479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65678105-A-T

121041148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65677863-C-T

121041392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65677625-C-T

121041468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65677549-T-A

121041514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65677504-A-G

121041977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675976-T-C

121041981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675972-C-T

http://identifiers.org/hco/4/GRCh38#121041990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65675962-A-C

121042057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675898-G-A

121042215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675733-C-T

121042368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675579-C-G

121042420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675534-T-A

121042518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675444-A-T

121042691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65675284-A-G

121043242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674829-T-C

121043371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674731-C-T

121043620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674502-T-C

http://identifiers.org/hco/4/GRCh38#121043890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65674269-A-C

http://identifiers.org/hco/4/GRCh38#121043925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65674235-C-A

121043966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674194-G-A

121043966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674194-G-C

121044020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674140-G-A

121044178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65674010-T-A

121044324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65673878-G-T

121044391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65673814-T-C

121045377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65673515-T-A

121045875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65672984-A-G

http://identifiers.org/hco/4/GRCh38#121045953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65672912-C-A

121045953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65672912-C-G

121045995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65672855-A-G

121050007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65671955-T-C

121050225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65671738-A-G

121050325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65671471-C-T

http://identifiers.org/hco/4/GRCh38#121050623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65670808-A-C

121050858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65670573-T-C

121051003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65670196-T-A

121051389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65669323-A-G

121051866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668903-T-A

121051866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668903-T-G

121051879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668890-T-C

121051901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668440-A-G

121051980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668384-A-G

121052080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668280-A-T

121052201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668149-G-T

121052218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668133-A-G

121052323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65668068-T-A

121052647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65667745-G-A

121052730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65667672-T-C

121052735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65667667-G-A

121052999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65667386-G-A

121053122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65667307-T-C

121053122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65667307-T-G

121053484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65666997-G-A

121054479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65666123-G-C

121054527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65666075-G-A

121054629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65665979-G-A

http://identifiers.org/hco/4/GRCh38#121055259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65665500-A-C

121055342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65665424-A-G

121055528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65665287-T-C

121056339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65664398-A-G

121056554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65664085-A-G

http://identifiers.org/hco/4/GRCh38#121056573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65664068-A-C

121057091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65663559-G-A

121057109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65663546-A-G

121057468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662646-C-G

121057468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662646-C-T

121057472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662642-G-A

121057544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662587-A-G

121057572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662560-G-A

http://identifiers.org/hco/4/GRCh38#121057598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65662533-A-C

121057691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662451-G-A

121057710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662432-C-G

121057774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662368-A-G

121057834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662315-G-T

121057860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662289-G-A

http://identifiers.org/hco/4/GRCh38#121057876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65662273-C-A

121057876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662273-C-G

121057894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662255-G-A

121057901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662248-T-C

121058040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662101-G-T

121058043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662098-C-T

121058066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65662075-G-C

121058183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661960-A-G

121058309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661829-A-G

121058351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661798-C-T

121058479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661689-G-A

121058595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661587-A-G

121058764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661440-C-G

121058809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661401-A-G

121058875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661359-C-T

121058902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661326-C-G

121058946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661281-T-A

121059064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661175-C-T

121059299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65661003-G-C

121059650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660637-C-T

121059818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660533-T-C

121059818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660533-T-G

121059886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660482-G-A

121059892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660476-G-A

121059892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660476-G-C

121061152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660322-A-G

http://identifiers.org/hco/4/GRCh38#121061180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65660295-C-A

121061196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65660278-A-G

121061207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65660267-T-C

http://identifiers.org/hco/4/GRCh38#121061208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65660266-C-A

121061208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65660266-C-T

121061535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660188-T-G

121061566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660157-A-G

http://identifiers.org/hco/4/GRCh38#121061592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65660131-C-A

121061694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65660036-T-C

http://identifiers.org/hco/4/GRCh38#121061798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65659974-A-C

121061819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65659954-C-G

121061825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65659948-T-G

121061856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65659913-A-G

121061876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65659897-T-A

121061876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65659897-T-C

121062021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65659785-A-G

http://identifiers.org/hco/4/GRCh38#121063073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65658198-C-A

121063074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65658197-A-G

121063076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65658195-T-C

121063215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65658078-C-T

http://identifiers.org/hco/4/GRCh38#121063227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65658066-C-A

121063538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657710-T-C

121063542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657706-T-C

http://identifiers.org/hco/4/GRCh38#121063734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65657519-C-A

121063734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657519-C-T

121063751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657502-G-A

121063850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657399-T-C

121063967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657290-A-T

121064064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65657016-A-T

121064229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65656860-T-C

121064231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65656858-G-A

121064236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65656853-T-C

121066636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65654871-C-T

121066811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65654460-A-G

121066893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65654382-G-C

121067130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65654163-G-A

121067718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653507-A-T

121067757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653460-A-G

121067762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653455-T-A

121067785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653436-T-C

121067858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653364-T-C

121067877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653345-G-T

121068084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653189-T-C

121068241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653073-G-A

121068267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65653047-A-G

121068377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65652708-G-T

http://identifiers.org/hco/4/GRCh38#121068478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65652607-A-C

121068478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65652607-A-T

121068919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65652256-G-A

121069406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651798-T-A

121069406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651798-T-C

121069572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651660-T-A

121069572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651660-T-G

121069627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651605-C-G

121069685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651551-G-A

121069685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651551-G-T

http://identifiers.org/hco/4/GRCh38#121069804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65651158-C-A

121069804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65651158-C-G

121069961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650988-T-C

121070095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650853-T-C

121070099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650849-G-A

121070099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650849-G-T

121070248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650697-G-A

121070375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650555-C-T

121070569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650337-G-A

121070600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650307-G-A

121070600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65650307-G-C

121071047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65649933-C-T

121071130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65649850-G-A

http://identifiers.org/hco/4/GRCh38#121071183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65649807-A-C

121071183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron variant
orthologous variants: 65649807-A-G

121071270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65649714-C-T

121071330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65649662-G-A

121071409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 65649581-T-C

121071452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65649532-G-T

http://identifiers.org/hco/4/GRCh38#121071475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65649499-C-A

121071475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65649499-C-T

121071521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65649457-G-A

121071521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 65649457-G-T

121071591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65649387-A-G

121071627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65649355-G-A

121071627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65649355-G-T

http://identifiers.org/hco/4/GRCh38#121071629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65649353-C-A

http://identifiers.org/hco/4/GRCh38#121071697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65649293-C-A

http://identifiers.org/hco/4/GRCh38#121071705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65649285-C-A

121071705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65649285-C-T

http://identifiers.org/hco/4/GRCh38#121071752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65649261-A-C

121071873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65649195-G-A

121072047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65649009-G-A

121072100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65648957-A-G

121072100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65648957-A-T

121072126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65648938-G-A

121072460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65648667-G-A

121072460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 65648667-G-T

121072718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65648423-A-T

121072720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65648421-A-T

121072746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65648395-A-G

121072746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65648395-A-T

121072750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 65648391-A-G

121072861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648292-G-A

121072861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648292-G-T

121072902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648223-C-T

121072926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648194-C-T

121072973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648147-G-A

121072973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648147-G-T

http://identifiers.org/hco/4/GRCh38#121072996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#65648125-C-A

121072996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 65648125-C-T