127965321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801326-G-A

127965321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801326-G-C

127965323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801328-G-A

127965323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801328-G-C

127965323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801328-G-T

http://identifiers.org/hco/4/GRCh38#127965417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801387-C-A

127965417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801387-C-T

127965424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801394-G-A

127965424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801394-G-T

127965446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801415-T-C

http://identifiers.org/hco/4/GRCh38#127965448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801417-C-A

127965448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801417-C-T

127965452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801421-T-C

127965469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801437-T-C

127965478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801445-G-T

http://identifiers.org/hco/4/GRCh38#127965531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801498-C-A

127965531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801498-C-G

127965531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801498-C-T

127965541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801503-G-C

127965573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801535-G-A

127965573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801535-G-T

http://identifiers.org/hco/4/GRCh38#127965580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801542-C-A

127965580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801542-C-G

127965580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801542-C-T

http://identifiers.org/hco/4/GRCh38#127965582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801544-A-C

127965582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801544-A-G

http://identifiers.org/hco/4/GRCh38#127965595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801557-A-C

127965595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801557-A-T

127965598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801560-T-C

127965618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801591-G-A

127965624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801597-T-C

127965641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801614-T-G

127965677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801631-C-T

127965688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801642-A-G

127965692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801646-A-T

127965704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801658-G-A

127965704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801658-G-T

127965716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801684-A-G

127965758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801727-G-A

127965758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801727-G-T

http://identifiers.org/hco/4/GRCh38#127965760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801729-C-A

127965760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801729-C-G

127965769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801738-A-G

127965774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801743-G-A

127965774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801743-G-T

127965790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801759-G-T

127965798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801767-T-C

http://identifiers.org/hco/4/GRCh38#127965819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801787-C-A

127965819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801787-C-T

127965853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801804-T-C

http://identifiers.org/hco/4/GRCh38#127965959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#40801867-C-A

127965959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801867-C-G

127965959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801867-C-T

127965995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40801877-G-T

127966055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 40801905-A-G

127966122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 40801958-A-G

127966141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40801972-G-A

127966251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802064-T-A

127966307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802121-A-G

127966309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802123-A-G

127966332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802146-T-C

127966334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802148-T-G

127966426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802218-A-G

127966514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802301-T-G

127967134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802587-A-G

127967309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802761-C-T

127967370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40802821-C-G

127967747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40803128-A-G

http://identifiers.org/hco/4/GRCh38#127968664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40804283-C-A

http://identifiers.org/hco/4/GRCh38#127968757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40804386-A-C

127968815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40804439-C-T

http://identifiers.org/hco/4/GRCh38#127968994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40804814-A-C

127968994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40804814-A-G

127969095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40804915-G-C

127972940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807388-A-G

127973402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807546-G-T

127973429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807565-C-G

127973429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807565-C-T

127973445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807580-T-C

127973592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807707-C-T

127973706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807950-T-C

127973707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40807951-G-C

127973806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40808055-C-G

http://identifiers.org/hco/4/GRCh38#127973817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40808066-C-A

http://identifiers.org/hco/4/GRCh38#127973818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40808067-A-C

127973858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40808080-G-A

127973858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40808080-G-T

127981951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40857891-A-G

127982461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40858885-C-T

http://identifiers.org/hco/4/GRCh38#127982484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40858908-A-C

127982484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40858908-A-G

127982498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40858922-A-T

127982813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40859203-T-C

127982964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40859345-G-A

127982964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40859345-G-C

127982964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40859345-G-T

127983143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40859786-G-T

127983163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40859814-A-G

127984105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860076-A-G

http://identifiers.org/hco/4/GRCh38#127984181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40860152-A-C

127984302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860269-A-G

127984302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860269-A-T

127984313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860280-C-G

127984313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860280-C-T

127984320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860295-G-T

127984324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860299-T-C

127984408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 40860376-A-G

127984428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860396-T-C

127984428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860396-T-G

127985312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40860895-G-T

http://identifiers.org/hco/4/GRCh38#127989660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40864879-C-A

127989662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40864881-A-G

127989675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40864892-A-G

127989703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40864921-G-C

127989703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40864921-G-T

127989715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 40864932-T-C

127989729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 40864946-G-A

127989729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 40864946-G-T

127989814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 40865031-A-T

127989827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40865044-A-G

127990213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40865266-T-A

127990539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40865606-G-A

128008932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 40871133-T-C

128008933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40871134-G-C

128009026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871230-T-G

128009074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871274-T-C

128009082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871282-A-G

128009103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 40871303-T-G

128009120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40871320-G-A

128009120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40871320-G-T

128009210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871410-T-C

128009210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871410-T-G

128009302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871537-A-G

128009306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40871541-G-T

http://identifiers.org/hco/4/GRCh38#128009309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40871544-C-A

128009388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40872588-C-T

128009514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40872697-G-A

128009514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40872697-G-C

128009515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40872698-T-C

128009519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40872702-G-A

http://identifiers.org/hco/4/GRCh38#128009541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40872720-A-C

http://identifiers.org/hco/4/GRCh38#128009568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40872747-C-A

128009625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40872781-A-G

128009973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40872983-A-G

128010054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873029-T-C

128010061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873036-C-T

128010093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873066-G-A

128010456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873424-G-C

128010515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873471-G-A

128010547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873503-G-A

128011460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873615-G-T

http://identifiers.org/hco/4/GRCh38#128011468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40873625-C-A

128011479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873636-G-T

128011503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873645-A-G

128011503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873645-A-T

128011565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873706-G-A

128011565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873706-G-T

128011587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873722-G-A

128011587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873722-G-T

128011595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873731-T-C

128011619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40873763-A-T

http://identifiers.org/hco/4/GRCh38#128011689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40873829-C-A

128011689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 40873829-C-G

128011689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 40873829-C-T

128011710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873850-T-C

128011786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873919-T-A

128011786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873919-T-C

128011786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873919-T-G

http://identifiers.org/hco/4/GRCh38#128011790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40873923-A-C

128011790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873923-A-G

128011790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873923-A-T

128011794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873927-G-A

128011794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873927-G-C

128011794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873927-G-T

128011859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40873962-A-G

128013947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40874838-G-A

128015328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40875962-G-C

128015332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40875966-G-C

128017353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 40877838-G-A

128017532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40878012-T-C

128017555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40878030-A-G

128017558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40878033-G-A

128017558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40878033-G-T

128019975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40884468-T-G

128020435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40884910-T-C

http://identifiers.org/hco/4/GRCh38#128020553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40885011-C-A

128020610-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40885061-T-A

128020645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40885096-T-C

128021245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 40885424-A-G

128028197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40887449-A-G

128028418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40887907-A-T

128028610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40888094-G-A

128028610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40888094-G-T

http://identifiers.org/hco/4/GRCh38#128028708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40888192-A-C

128028727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40888211-A-G

128028737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40888221-A-G

128028785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 40888269-T-C

128028891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40888386-T-C

128028893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40888388-T-A

128030717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 40889505-T-C

http://identifiers.org/hco/4/GRCh38#128035663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40889693-C-A

128035663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40889693-C-T

128035682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40889711-G-A

128035682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40889711-G-T

128035706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40889725-G-A

http://identifiers.org/hco/4/GRCh38#128035713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40889735-C-A

128035713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 40889735-C-T

http://identifiers.org/hco/4/GRCh38#128035833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40889848-C-A

128035833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40889848-C-T

128035857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40889865-A-G

http://identifiers.org/hco/4/GRCh38#128035869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40889875-C-A

128035972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40889974-G-A

128035972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40889974-G-T

128036494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890410-G-A

128036494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890410-G-T

128036499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890415-A-G

128036536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890470-G-T

128036642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890559-G-A

128036642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890559-G-T

128037918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40890970-A-G

128038625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891476-T-C

128038628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891479-C-G

128038628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891479-C-T

128038729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891567-A-T

128038764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891610-G-A

128038764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891610-G-C

128038764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891610-G-T

128038774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891620-G-C

128038788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891631-T-C

http://identifiers.org/hco/4/GRCh38#128038832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40891743-C-A

128038832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891743-C-G

128038832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891743-C-T

http://identifiers.org/hco/4/GRCh38#128038908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#40891828-C-A

128039016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40891964-A-G

128039146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40892136-T-C

128039293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26111
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 40892307-T-C