23992812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 12751804-G-A

23992877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5 prime UTR variant
orthologous variants: 12751863-A-G

23993174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12752104-T-C

23993348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12752596-G-A

23993385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12752634-T-C

http://identifiers.org/hco/18/GRCh38#23994056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12757692-A-C

23994056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12757692-A-G

http://identifiers.org/hco/18/GRCh38#23994220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12757855-C-A

23994220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12757855-C-T

23994287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12757988-T-A

23994305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12758007-T-A

23994305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12758007-T-C

http://identifiers.org/hco/18/GRCh38#23994312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12758014-C-A

23994312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12758014-C-T

23994360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12758120-G-A

23994394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12758136-T-C

23994447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12758189-G-T

23994481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12758226-T-C

23994511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12758265-G-A

23994546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12758300-C-G

23994546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12758300-C-T

23994573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12758327-A-G

23998211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12760926-G-A

23998730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12761299-G-A

23998803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12761372-T-C

http://identifiers.org/hco/18/GRCh38#23998806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12761375-A-C

23999268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12761865-G-C

23999389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12761978-C-T

http://identifiers.org/hco/18/GRCh38#23999492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12762113-C-A

23999492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12762113-C-T

23999638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12762688-C-T

http://identifiers.org/hco/18/GRCh38#23999641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12762691-C-A

23999769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12762798-G-T

23999843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12762873-T-C

24000077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763135-G-A

24000312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763374-G-T

24000582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763607-A-G

24000624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763648-T-G

http://identifiers.org/hco/18/GRCh38#24000647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12763662-A-C

24000662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763685-G-A

24000662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763685-G-T

24000673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763696-C-T

24000848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12763875-G-T

24000980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764005-C-T

24001038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764065-A-G

http://identifiers.org/hco/18/GRCh38#24001236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12764265-A-C

24001237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764266-A-G

http://identifiers.org/hco/18/GRCh38#24001430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12764453-A-C

24001446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764468-T-C

24002218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12764599-A-G

24002750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765357-G-A

http://identifiers.org/hco/18/GRCh38#24002797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12765402-A-C

24002897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765491-C-T

24003058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765634-G-C

24003272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12765803-C-T

24003512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12766033-C-T

24004581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768005-T-G

24004670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768410-T-C

24004708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12768443-G-C

24006850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12770330-T-C

24006860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12770340-C-T

24009827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12772936-G-A

24010572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12773241-C-T

24011763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12773937-A-G

24012115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774275-C-T

24012162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774338-T-C

24012464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12774661-T-C

24012836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775015-G-A

24012836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775015-G-T

24012934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12775086-T-C

24013105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775242-A-G

24013267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12775368-T-C

24013852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12776100-A-G

24014287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12776484-G-T

24014429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12776583-G-T

http://identifiers.org/hco/18/GRCh38#24014430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12776584-C-A

24014430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12776584-C-T

http://identifiers.org/hco/18/GRCh38#24014584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12776714-C-A

24014584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12776714-C-G

24014584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12776714-C-T

24014650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12776754-G-C

24014650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12776754-G-T

http://identifiers.org/hco/18/GRCh38#24014796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12776866-C-A

24014796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12776866-C-T

24014803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12776873-C-T

24014852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12776923-G-A

24014852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12776923-G-T

http://identifiers.org/hco/18/GRCh38#24014887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12776958-C-A

24014887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 12776958-C-T

http://identifiers.org/hco/18/GRCh38#24014893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12776964-C-A

24014893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12776964-C-G

24014893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12776964-C-T

http://identifiers.org/hco/18/GRCh38#24015000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12777062-C-A

24015000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 12777062-C-T

24015258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777285-G-A

24015258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777285-G-T

http://identifiers.org/hco/18/GRCh38#24015270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12777297-C-A

24015270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777297-C-T

http://identifiers.org/hco/18/GRCh38#24015276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12777303-C-A

http://identifiers.org/hco/18/GRCh38#24015283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12777310-C-A

24015283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777310-C-G

24015283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777310-C-T

24015488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777511-T-C

24015659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12777673-C-T

24015677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12777691-G-A

24015738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12777738-T-A

24015898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12777868-G-A

24016519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778620-T-A

24016519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778620-T-C

24016521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778622-A-G

24016682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12778772-T-C

24016763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778878-G-C

24016763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778878-G-T

24016764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778879-G-T

24016822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12778927-A-T

24017117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12779170-G-A

24017142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12779192-G-T

24017669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780076-T-G

24017739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780146-A-G

24017739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780146-A-T

24017740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780147-T-C

24017871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780254-T-C

24018062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12780416-A-G

24018677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12781299-G-C

24018766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12781378-G-A

24018867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12781458-G-A

24019455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782299-A-G

24019481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782324-G-T

24019723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12782560-A-G

24019757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782596-G-C

24019757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782596-G-T

24019814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782656-A-G

24019814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782656-A-T

http://identifiers.org/hco/18/GRCh38#24019820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12782658-C-A

24019820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782658-C-T

24019822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782660-T-C

24019888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782700-T-C

24019901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782713-G-T

24020010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782815-G-A

24020010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782815-G-C

24020077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782856-G-A

24020077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782856-G-C

24020077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782856-G-T

http://identifiers.org/hco/18/GRCh38#24020080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12782859-A-C

24020090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782869-A-G

24020096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782875-G-A

24020096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12782875-G-T

24020145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782902-G-T

24020187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782933-C-G

24020207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782953-G-C

24020207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782953-G-T

http://identifiers.org/hco/18/GRCh38#24020226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12782973-C-A

24020226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782973-C-T

24020246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12782990-C-T

http://identifiers.org/hco/18/GRCh38#24020277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12783021-A-C

24020316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783065-C-G

24020316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783065-C-T

24020334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783083-A-G

24020354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783111-A-T

24020382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783149-G-A

24020399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783168-T-C

24020400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783169-G-A

24020400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783169-G-C

http://identifiers.org/hco/18/GRCh38#24020434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12783204-C-A

24020434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12783204-C-T

24022615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12783658-A-G

24025683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787048-C-T

24025731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787108-G-A

24025731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787108-G-T

24025848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787204-A-G

24025857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787211-G-A

24025885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787236-A-G

24025920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787271-G-A

24025920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787271-G-T

24026168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787523-T-A

24026217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787582-A-G

24026271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787644-A-G

24026563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787887-C-T

24026572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787895-A-G

24026616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12787928-T-C

24027293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788256-C-T

http://identifiers.org/hco/18/GRCh38#24027304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12788266-A-C

24027554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12788514-G-A

24028086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788734-T-C

24028333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12788978-G-A

24028395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789026-G-A

24028658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12789266-T-C

24038800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12792383-G-C

24038973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12792493-A-T

24039406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12792910-A-G

24039719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793224-G-A

24039892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793383-C-T

24039964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793466-G-A

24040050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793550-T-C

24040503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12793936-T-A

24040783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794157-G-C

http://identifiers.org/hco/18/GRCh38#24040857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12794252-A-C

24041213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794589-G-A

24041246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794622-A-G

24041370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794743-G-A

24041526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794890-T-C

24041537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794901-G-A

http://identifiers.org/hco/18/GRCh38#24041564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12794934-A-C

24041595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12794964-T-C

24041843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795305-T-C

24041905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795363-A-G

24041965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795416-A-G

24042054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795503-A-G

24042112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795547-A-G

24042123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12795558-A-G

24044166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797143-G-A

24044379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797341-G-C

24044386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797348-G-A

24044479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797390-G-A

24044636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797525-G-A

24044801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12797653-T-C

24046973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802341-C-G

24046981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802349-T-C

24046992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802359-G-A

24047277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802634-A-T

24047318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802691-C-G

24047375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802752-G-A

24047537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802910-T-C

24047585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12802957-C-T

24047816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12803322-G-C

24047837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12803343-A-G

24048315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12803629-G-A

24049316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804585-A-G

24049404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804669-C-T

24049481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804733-C-G

24049618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804846-C-T

24049645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804888-C-G

24049689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804913-A-G

24049698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12804927-G-T

http://identifiers.org/hco/18/GRCh38#24049737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12804971-A-C

24053068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807089-A-G

24053099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807119-A-G

24053101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807121-G-A

24053149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807165-C-T

24053203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807212-A-G

24053203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807212-A-T

24053255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12807260-T-C

24054135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12808543-T-C

24054357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12808721-C-T

24054391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12808758-A-G

24056279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12811315-T-A

24056282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12811318-A-T

24056347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12811377-G-A

24056347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12811377-G-T

24056354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12811384-G-A

24056354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12811384-G-T

http://identifiers.org/hco/18/GRCh38#24056617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12811860-C-A

24056772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12812024-C-T

24061984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816054-C-T

24062018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12816068-C-T

24062019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12816069-G-A

24062019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12816069-G-C

24062033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816083-C-T

24062075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816123-T-C

24062082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816130-G-A

24062122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816167-G-A

24062306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816306-G-A

24062630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12816595-G-T

24063312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817373-A-G

24063531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817469-G-T

24063533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817471-G-A

24063533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817471-G-C

24063533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817471-G-T

24063598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817507-C-T

24063911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12817707-G-T

24064322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12818050-G-A

24064322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12818050-G-T

24064409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12818136-T-A

24064524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12818238-T-C

24064524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12818238-T-G

http://identifiers.org/hco/18/GRCh38#24064748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12818418-A-C

http://identifiers.org/hco/18/GRCh38#24064857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12818519-A-C

24064857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12818519-A-G

24065105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819073-G-T

24065187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819160-G-A

24065276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819255-G-C

24065328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819310-G-A

24065345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819316-G-A

24065521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819544-A-G

24065544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819567-A-G

24065890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819892-T-C

http://identifiers.org/hco/18/GRCh38#24065988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12819985-C-A

24065988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819985-C-G

24065988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12819985-C-T

24066014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 12820011-T-C

http://identifiers.org/hco/18/GRCh38#24066053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12820050-A-C

24066053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12820050-A-T

24066125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12820122-T-C

24066166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820157-G-A

24066166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12820157-G-T

24067229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822209-C-T

24067230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822210-G-A

24067983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12821680-A-G

24068044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12821723-G-A

24068325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12821974-C-T

24068341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12821990-T-C

24068481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822128-G-A

24068563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822209-C-T

24068564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822210-A-G

24068723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822370-C-T

24069076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822730-G-A

24069076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822730-G-T

24069089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822754-A-T

24069282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822955-G-A

24069282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822955-G-C

24069321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12822992-T-G

http://identifiers.org/hco/18/GRCh38#24069329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12823005-A-C

24069370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823048-A-G

24069393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823073-A-T

24069647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12823323-C-T

24070055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824037-T-C

24070099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824058-T-G

http://identifiers.org/hco/18/GRCh38#24070218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12824158-A-C

http://identifiers.org/hco/18/GRCh38#24070312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12824267-A-C

24070437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824392-T-C

24070533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12824495-G-A

24073297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12825504-T-G

24080553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12828260-T-C

http://identifiers.org/hco/18/GRCh38#24080569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12828277-C-A

24080569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12828277-C-G

24080569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12828277-C-T

24080758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12828466-C-G

24080958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12828666-A-G

24081050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12828757-G-A

24081050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12828757-G-T

24081203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829281-T-A

24081216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829291-G-A

24081374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829445-G-A

24081391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829462-C-T

24081394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829465-T-A

24081618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829841-G-T

24081682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829881-G-A

24081796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829984-G-A

24081796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12829984-G-T

24081915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830105-G-C

24082043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830209-A-G

24082043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830209-A-T

24082303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830321-G-T

24082477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830594-G-A

24082551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830639-A-G

24082551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830639-A-T

24082689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830736-C-T

24082820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830848-G-A

24082820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830848-G-T

24082857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12830889-T-G

http://identifiers.org/hco/18/GRCh38#24083119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12831152-C-A

24083119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831152-C-G

24083119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831152-C-T

24083125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831158-T-A

24083698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12831303-G-T

http://identifiers.org/hco/18/GRCh38#24087507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12833810-A-C

http://identifiers.org/hco/18/GRCh38#24088197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12834482-C-A

24089001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836588-G-A

24089001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836588-G-T

24089091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12836674-C-T

24089510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12837045-G-A

24089510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12837045-G-C

http://identifiers.org/hco/18/GRCh38#24089780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12837310-C-A

24089973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12840126-C-G

24102369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12844139-A-G

24110699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12847187-T-C

24110728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12847213-C-G

24110728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12847213-C-T

24112238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12848989-A-T

24112345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12849050-C-T

24112380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12849076-T-C

24112901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, undefined
orthologous variants: 12849476-T-A

24112912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12849495-C-T

http://identifiers.org/hco/18/GRCh38#24112918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12849501-C-A

24113007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12849700-C-G

24113007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron variant
orthologous variants: 12849700-C-T

24113174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, undefined
orthologous variants: 12849866-A-G

24113207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, undefined
orthologous variants: 12849899-T-G

http://identifiers.org/hco/18/GRCh38#24113208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12849900-A-C

http://identifiers.org/hco/18/GRCh38#24113322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12850006-C-A

24113322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, undefined
orthologous variants: 12850006-C-T

http://identifiers.org/hco/18/GRCh38#24113427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12850054-C-A

24113427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 12850054-C-T

http://identifiers.org/hco/18/GRCh38#24113433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12850060-C-A

24113433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 12850060-C-T

24113511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12850134-A-G

24113532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12850147-G-A

24113532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12850147-G-T

24113546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12850159-C-T

24113566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12850188-G-A

http://identifiers.org/hco/18/GRCh38#24113586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12850209-A-C

24113651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12850280-A-T

http://identifiers.org/hco/18/GRCh38#24113737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12850338-C-A

24113827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12851763-A-G

http://identifiers.org/hco/18/GRCh38#24113882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12851816-A-C

24113884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12851818-G-A

24113884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12851818-G-T

http://identifiers.org/hco/18/GRCh38#24113898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12851832-A-C

http://identifiers.org/hco/18/GRCh38#24113907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12851841-C-A

24113907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12851841-C-G

24114023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12851954-A-G

24114023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12851954-A-T

24114102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12852019-G-A

24114102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12852019-G-T

24114149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852065-G-T

http://identifiers.org/hco/18/GRCh38#24114160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12852076-A-C

24114160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852076-A-G

24114160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852076-A-T

http://identifiers.org/hco/18/GRCh38#24114178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12852094-A-C

24114178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852094-A-G

24114178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852094-A-T

24114189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852102-T-C

24114189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852102-T-G

24114196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852109-G-A

24114196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852109-G-C

24114196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852109-G-T

24114208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852126-T-C

24114208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852126-T-G

24114219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852137-G-A

24114219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852137-G-C

24114368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12852834-T-G

24114395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12852854-C-T

http://identifiers.org/hco/18/GRCh38#24114548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12853001-C-A

24114548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12853001-C-G

24114548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12853001-C-T

24114628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12853081-T-A

24115525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855482-T-C

24115934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855858-G-A

24115934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12855858-G-T

24116649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856170-A-G

24116723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12856357-G-A

24118060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857932-G-T

24118085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857956-A-G

24118090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857961-T-C

24118093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857964-A-G

24118094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857965-G-A

24118094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12857965-G-T

24118126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 12857997-T-C

24119408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859892-C-T

24119463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859961-T-C

24119482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859980-G-A

24119482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12859980-G-T

http://identifiers.org/hco/18/GRCh38#24119596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12860084-A-C

24119854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12860321-T-C

24119858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12860325-T-C

24119947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12860414-A-G

24119975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12860437-A-T

24123802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12861646-T-G

24123916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12861759-T-G

http://identifiers.org/hco/18/GRCh38#24123986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12861833-C-A

24123986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861833-C-T

24124359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861977-G-A

24124359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12861977-G-T

http://identifiers.org/hco/18/GRCh38#24124410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12862028-C-A

24124410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862028-C-G

24125270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862908-A-G

24125369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12862992-A-G

http://identifiers.org/hco/18/GRCh38#24125513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12863137-A-C

http://identifiers.org/hco/18/GRCh38#24128792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12865925-C-A

24128857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865986-C-T

24128861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865990-T-C

http://identifiers.org/hco/18/GRCh38#24128869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12865998-C-A

24128869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12865998-C-T

24128882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12866011-T-C

24128882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12866011-T-G

24128908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12866037-A-G

24128908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12866037-A-T

24128996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866120-T-C

24129009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866133-A-G

24129020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866144-G-A

24129020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866144-G-T

http://identifiers.org/hco/18/GRCh38#24129024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12866148-C-A

24129024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866148-C-G

24129024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866148-C-T

http://identifiers.org/hco/18/GRCh38#24129028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12866152-C-A

http://identifiers.org/hco/18/GRCh38#24129067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12866192-C-A

24129067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866192-C-T

http://identifiers.org/hco/18/GRCh38#24129074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12866199-C-A

24129074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866199-C-G

24129074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866199-C-T

24129102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866229-A-G

24129102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866229-A-T

24129114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866242-G-T

24129124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866252-A-G

24129147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866274-A-T

24129179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12866308-A-G

24130167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867820-G-T

24130271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867905-T-C

http://identifiers.org/hco/18/GRCh38#24130289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12867922-C-A

24130289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12867922-C-T

24130348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12867979-T-C

24130363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12867994-T-C

24130379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12868010-T-C

24130423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868059-A-T

http://identifiers.org/hco/18/GRCh38#24130490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12868107-C-A

24130490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12868107-C-T

http://identifiers.org/hco/18/GRCh38#24130566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12868166-C-A

24131928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12869083-T-C

24131938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869098-A-G

24131999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869159-G-T

http://identifiers.org/hco/18/GRCh38#24132351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12869600-A-C

24132422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12869667-A-T

24132762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12870000-G-T

24132995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12870218-T-A

24133070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12870373-A-G

24133245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12870541-A-G

24133597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12871314-G-T

24133662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12871375-A-G

24133689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12871402-T-C

24133875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12871569-T-C

http://identifiers.org/hco/18/GRCh38#24133913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12871612-A-C

24134146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12871941-G-A

24134783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12872195-T-A

24134799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26595
most severe consequence: 3 prime UTR variant
orthologous variants: 12872211-G-A