http://identifiers.org/hco/12/GRCh38#47753999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97661486-C-A

http://identifiers.org/hco/12/GRCh38#47754172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97661710-C-A

47754173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97661711-T-C

47754216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97661750-C-T

47754393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97661903-C-T

47754828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97662505-A-G

http://identifiers.org/hco/12/GRCh38#47755718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97663035-C-A

47755718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663035-C-T

47756011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663210-A-G

47756082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663268-G-T

47756112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663298-A-G

http://identifiers.org/hco/12/GRCh38#47756167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97663330-C-A

http://identifiers.org/hco/12/GRCh38#47756169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97663332-C-A

47756170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663333-T-A

47756170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663333-T-C

47756170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663333-T-G

47756206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663364-T-C

http://identifiers.org/hco/12/GRCh38#47756228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97663386-C-A

47756228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663386-C-G

47756239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663397-G-T

47756249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663407-G-A

47756271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97663430-C-G

http://identifiers.org/hco/12/GRCh38#47756338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97663496-C-A

47756394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663544-C-T

http://identifiers.org/hco/12/GRCh38#47756453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97663587-C-A

47756453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663587-C-T

47756467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97663617-G-T

47756490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97663639-G-T

47756602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97663731-A-T

47757063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97663987-G-C

47757399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97664198-A-G

47757526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97664323-G-A

47757526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97664323-G-C

http://identifiers.org/hco/12/GRCh38#47757741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97664544-C-A

47757741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97664544-C-G

47757741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97664544-C-T

http://identifiers.org/hco/12/GRCh38#47757872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97664649-C-A

47757872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97664649-C-G

47757872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97664649-C-T

47757884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97664661-G-A

47757884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97664661-G-C

47758009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97664786-G-A

47758009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97664786-G-C

47758009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97664786-G-T

http://identifiers.org/hco/12/GRCh38#47758021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97664798-C-A

47758021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97664798-C-T

47758043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97664820-G-A

47758043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97664820-G-T

47758098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97664875-G-A

47758098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97664875-G-C

47758098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97664875-G-T

47758123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97664894-G-C

47758123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97664894-G-T

47758284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97665048-G-A

47758284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97665048-G-T

47758436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97665178-T-A

47758727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97665420-G-A

47758727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97665420-G-T

http://identifiers.org/hco/12/GRCh38#47758743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97665437-C-A

47758743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97665437-C-T

47758816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97665507-G-C

47758816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97665507-G-T

http://identifiers.org/hco/12/GRCh38#47758916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97665608-C-A

47758916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97665608-C-G

47758916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97665608-C-T

http://identifiers.org/hco/12/GRCh38#47758949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97665639-C-A

47758949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97665639-C-T

47759041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97665728-G-A

47759041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97665728-G-T

http://identifiers.org/hco/12/GRCh38#47759243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97665921-A-C

47759243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97665921-A-G

47759344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97666023-C-G

47759344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97666023-C-T

47759508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97666174-T-G

47759554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97666217-C-T

47759871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97666510-G-C

http://identifiers.org/hco/12/GRCh38#47760078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97666579-A-C

47760078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97666579-A-T

47760099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97666600-A-T

47760223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 97666729-G-A

47760223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 97666729-G-T

47760254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666760-A-G

47760264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666770-G-A

47760264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666770-G-T

47760292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666798-G-T

47760336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666832-G-C

47760336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666832-G-T

47760392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 97666866-G-A

47760392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained
orthologous variants: 97666866-G-T

http://identifiers.org/hco/12/GRCh38#47760435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97666905-A-C

47760435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97666905-A-T

http://identifiers.org/hco/12/GRCh38#47760546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97667001-C-A

47760546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97667001-C-T

47761361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668557-A-G

47761386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668582-G-A

47761386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668582-G-C

47761531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668691-C-T

47761592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668750-C-T

http://identifiers.org/hco/12/GRCh38#47761605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97668763-A-C

47761730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668891-G-A

47761837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668981-A-T

47761838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668982-C-G

47761838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97668982-C-T

47762009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97669143-C-T

47762033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97669168-A-G

47762114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97669269-A-T

47762134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97669289-T-A

47762776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670124-A-G

47762992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670581-C-T

47763017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670605-C-G

47763023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670611-C-T

47763033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670622-G-C

47763144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670722-G-T

47763154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97670732-C-T

47763916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97671384-A-G

47764011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97671459-G-A

47764107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97671536-G-T

http://identifiers.org/hco/12/GRCh38#47764114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97671544-C-A

47764483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97671937-G-A

47764495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97671949-G-T

47764536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97671980-G-A

47765393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97672704-C-T

47765397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97672708-G-A

47765430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97672747-C-T

47765484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97672801-G-A

http://identifiers.org/hco/12/GRCh38#47765533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97672826-A-C

47765789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673053-G-A

47765789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673053-G-T

47765810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97673073-C-G

47765810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97673073-C-T

http://identifiers.org/hco/12/GRCh38#47765956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97673180-C-A

47765994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673224-G-A

47765994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673224-G-T

47766001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673229-T-C

47766002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673230-A-G

47766012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673240-T-C

47766489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673695-G-C

http://identifiers.org/hco/12/GRCh38#47766512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97673721-A-C

47766658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673931-C-G

47766662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97673935-G-T

47767073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97674355-T-C

47767118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97674383-A-G

47767169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97674439-G-T

47767343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97674606-T-C

http://identifiers.org/hco/12/GRCh38#47768436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97676491-C-A

47768436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97676491-C-T

47768560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97676609-A-G

47768560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97676609-A-T

47768624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97676672-T-C

47768805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97676836-G-C

47768878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97676894-T-C

http://identifiers.org/hco/12/GRCh38#47768911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97676921-A-C

47768975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97676986-A-G

47769038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97677048-G-A

47769077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97677085-G-T

http://identifiers.org/hco/12/GRCh38#47769118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97677124-C-A

http://identifiers.org/hco/12/GRCh38#47769122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97677128-C-A

47769500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97677902-T-C

47769516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97677919-T-C

47769535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97677937-T-C

47769608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97678002-G-A

http://identifiers.org/hco/12/GRCh38#47769681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97678064-C-A

http://identifiers.org/hco/12/GRCh38#47769714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97678081-C-A

47769781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97678144-G-A

47769781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97678144-G-T

http://identifiers.org/hco/12/GRCh38#47770177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97678493-C-A

47770764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97679140-G-T

http://identifiers.org/hco/12/GRCh38#47770813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97679273-C-A

47770813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97679273-C-G

47770819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97679279-T-A

47770819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97679279-T-C

47770923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97679393-G-C

47770923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 97679393-G-T

47771247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97680030-T-C

47771249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97680032-T-C

http://identifiers.org/hco/12/GRCh38#47771268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97680052-A-C

47771281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97680064-C-T

http://identifiers.org/hco/12/GRCh38#47771437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97680208-C-A

47771437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97680208-C-T

http://identifiers.org/hco/12/GRCh38#47771462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97680225-C-A

47771541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron variant
orthologous variants: 97680290-G-T

47773066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97682157-G-T

47773164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97682227-G-A

47773164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97682227-G-C

47773164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97682227-G-T

47773165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: intron_variant, undefined
orthologous variants: 97682228-C-T

http://identifiers.org/hco/12/GRCh38#47773271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97682342-C-A

47773271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97682342-C-G

47773271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97682342-C-T

http://identifiers.org/hco/12/GRCh38#47773498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97682542-C-A

47773807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97682816-C-G

47773981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97682904-G-A

47774530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97683490-A-T

47774643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97683756-G-A

47774973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684056-G-A

47775058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684141-T-C

47775058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684141-T-G

47775164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684211-A-T

47775816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684866-C-T

47775862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97684912-G-A

47776110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685154-G-A

47776164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685208-C-T

47776198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685213-C-T

http://identifiers.org/hco/12/GRCh38#47776309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97685282-A-C

47776611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685556-G-A

47776796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685676-C-T

47776834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97685722-C-T

47777122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686060-G-A

47777753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686578-C-T

47778092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686817-G-T

47778101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97686827-C-T

47778363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97687061-G-A

47778402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97687109-T-C

47778478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97687200-T-C

47778478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97687200-T-G

47778498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97687220-G-T

47778673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687339-A-G

47778747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687409-T-G

47778751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687413-G-T

47778804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687443-G-T

http://identifiers.org/hco/12/GRCh38#47778818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97687454-C-A

47778818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97687454-C-G

47778818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97687454-C-T

47778845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97687487-G-T

47778864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97687514-A-G

47778864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97687514-A-T

47778945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687655-T-C

47778964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687674-G-A

47778990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97687706-G-T

47779112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97687868-T-G

47779137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97687893-G-A

47779198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687954-G-A

http://identifiers.org/hco/12/GRCh38#47779210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97687964-C-A

47779210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687964-C-T

47779291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687987-G-C

47779291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97687987-G-T

http://identifiers.org/hco/12/GRCh38#47779311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97688010-C-A

47779311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97688010-C-T

47779326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97688025-T-C

47779341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97688040-T-C

47779341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 97688040-T-G

47779566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97688211-G-C

47779567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97688212-T-C

http://identifiers.org/hco/12/GRCh38#47779998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97688337-C-A

47780060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 97688396-G-A

47780308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688630-G-C

47780308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688630-G-T

47780360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688682-C-T

http://identifiers.org/hco/12/GRCh38#47780497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97688813-C-A

47780497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688813-C-T

47780505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688821-T-A

47780505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688821-T-C

47780506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688822-G-A

47780506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688822-G-C

47780511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 97688827-G-A

http://identifiers.org/hco/12/GRCh38#47781075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689162-C-A

http://identifiers.org/hco/12/GRCh38#47781076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689163-C-A

http://identifiers.org/hco/12/GRCh38#47781105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689182-C-A

47781134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689211-A-G

47781160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689229-A-G

47781167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689236-T-A

47781167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689236-T-C

http://identifiers.org/hco/12/GRCh38#47781207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689279-A-C

http://identifiers.org/hco/12/GRCh38#47781297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689370-C-A

47781297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689370-C-T

http://identifiers.org/hco/12/GRCh38#47781303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689375-A-C

47781303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689375-A-G

http://identifiers.org/hco/12/GRCh38#47781369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689412-C-A

http://identifiers.org/hco/12/GRCh38#47781563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689587-C-A

47781563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689587-C-T

47781657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689674-G-A

47781657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689674-G-T

47781695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689713-G-A

47781695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689713-G-T

http://identifiers.org/hco/12/GRCh38#47781770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689764-C-A

47781770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689764-C-T

47781787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689776-C-T

47781815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689793-G-A

47781815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689793-G-T

http://identifiers.org/hco/12/GRCh38#47781845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97689815-C-A

47781845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689815-C-G

47781845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689815-C-T

47781938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689881-G-T

47782051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689980-G-A

47782051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97689980-G-T

47782121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97690017-G-A

47782121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97690017-G-T

http://identifiers.org/hco/12/GRCh38#47782124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97690020-C-A

47782164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97690045-G-A

47782164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97690045-G-C

47782164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 97690045-G-T

47782239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690111-G-A

47782281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690152-C-T

47782287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690158-G-T

47782304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690175-A-G

47782310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690177-G-T

47782365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690240-G-A

47782365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690240-G-T

47782368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690243-T-C

47782370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690245-T-C

http://identifiers.org/hco/12/GRCh38#47782427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97690293-A-C

47782427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690293-A-T

47782472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690320-T-A

47782472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690320-T-C

http://identifiers.org/hco/12/GRCh38#47782505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97690351-C-A

47782505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690351-C-T

47782540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690370-G-A

47782598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690439-G-A

47782598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690439-G-T

47782613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690449-G-T

47782682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 97690502-C-T

47782705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26035
most severe consequence: 3 prime UTR variant
orthologous variants: 97690525-G-A