180602945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 33855159-G-A

http://identifiers.org/hco/3/GRCh38#180602960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33855174-A-C

180602960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 33855174-A-G

180603188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 33855404-G-A

180603256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 33855472-G-T

http://identifiers.org/hco/3/GRCh38#180603390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33855578-C-A

180603435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33855625-G-T

180604194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33856977-G-A

180604354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857129-T-A

180604452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857199-T-C

180604452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857199-T-G

http://identifiers.org/hco/3/GRCh38#180604618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33857363-C-A

180604618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857363-C-T

180604624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857371-A-G

180604728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857450-A-G

http://identifiers.org/hco/3/GRCh38#180604747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33857469-C-A

180604747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857469-C-G

180604815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857537-A-G

180605018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857766-T-C

http://identifiers.org/hco/3/GRCh38#180605106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33857845-C-A

180605106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857845-C-T

180605136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857875-G-T

180605211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857946-A-G

180605237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33857960-T-C

180605628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858023-T-G

180605681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858076-G-T

180605894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858271-G-C

180605894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858271-G-T

180605898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858275-A-G

180605910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858287-T-A

180606183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858501-T-G

180606237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33858555-C-G

180606641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33858949-G-A

180606641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33858949-G-T

http://identifiers.org/hco/3/GRCh38#180606647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33858955-C-A

180606647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33858955-C-T

180606690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33859004-G-A

180606690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33859004-G-C

180607166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33860367-T-C

180607233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33860564-G-A

180607462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33860800-A-T

180607582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, undefined
orthologous variants: 33860908-C-G

180607641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 33860958-A-T

180607908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33861204-G-A

180607908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33861204-G-C

180607908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33861204-G-T

http://identifiers.org/hco/3/GRCh38#180608007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33861307-A-C

180608007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 33861307-A-G

http://identifiers.org/hco/3/GRCh38#180608024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33861325-C-A

http://identifiers.org/hco/3/GRCh38#180608411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33861706-A-C

180608411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33861706-A-G

180608411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33861706-A-T

180608416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33861711-T-C

http://identifiers.org/hco/3/GRCh38#180608440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33861735-C-A

180608440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33861735-C-T

180608446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33861741-A-T

http://identifiers.org/hco/3/GRCh38#180608506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33861801-C-A

180608802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 33862089-A-G

180608835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862127-T-C

180608950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862223-A-T

180608961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862233-G-A

http://identifiers.org/hco/3/GRCh38#180608968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33862240-C-A

180608968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862240-C-T

180609076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862333-T-C

http://identifiers.org/hco/3/GRCh38#180609103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33862360-C-A

180609103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862360-C-G

180609127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862377-G-A

180609127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862377-G-T

180609208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862418-A-G

180609275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862480-A-T

180609284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862490-A-G

180609284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862490-A-T

180609314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862519-G-T

180609340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862549-T-C

180609340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862549-T-G

180609363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862574-G-A

180609363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862574-G-C

180609472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862676-A-G

180609474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862678-A-G

http://identifiers.org/hco/3/GRCh38#180609554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33862753-C-A

180609554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862753-C-T

180609607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862811-G-A

180609607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33862811-G-T

180609691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33862896-G-A

180609691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33862896-G-T

180609770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33862975-G-A

180609770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33862975-G-T

180609772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33862977-A-G

180610123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863310-T-G

180610130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863317-G-A

180610130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863317-G-C

180610166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863359-G-T

180610310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863503-G-A

180610357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863550-G-A

http://identifiers.org/hco/3/GRCh38#180610361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33863560-A-C

180610361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 33863560-A-T

180610362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 33863561-A-G

180610838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33863961-G-A

180610880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 33864007-G-T

180611033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 33864165-T-G

http://identifiers.org/hco/3/GRCh38#180611111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33864225-A-C

180611273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: 33864382-C-G

180611735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: 33864805-G-T

180611909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: 33864936-G-A

180612237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: 33865402-A-G

http://identifiers.org/hco/3/GRCh38#180613772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33866109-A-C

http://identifiers.org/hco/3/GRCh38#180613775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33866112-C-A

180613781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: 33866123-A-G

180613959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron variant
orthologous variants: 33866278-T-C

180614060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33866379-T-C

180614110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33866420-A-G

http://identifiers.org/hco/3/GRCh38#180614421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33866638-A-C

http://identifiers.org/hco/3/GRCh38#180614437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33866663-A-C

180614477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33866719-A-G

180614509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33866759-G-T

180614529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33866777-A-G

180614675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33866885-G-T

180614814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867039-A-G

180614814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867039-A-T

180614842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867071-A-T

180614867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867133-T-A

180614898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867176-T-A

180614898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867176-T-C

180614900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867178-T-C

180614902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867180-T-C

http://identifiers.org/hco/3/GRCh38#180614903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33867181-C-A

180614903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867181-C-T

180614904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33867182-A-G

180614922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: 33867197-T-A

http://identifiers.org/hco/3/GRCh38#180614991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33867266-C-A

180614991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33867266-C-T

180615048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33867329-G-A

180615048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33867329-G-T

180615107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33867381-A-G

http://identifiers.org/hco/3/GRCh38#180615191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33867465-C-A

180615191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33867465-C-T

180615213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33867487-T-C

180615385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33867609-A-G

180615499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33867708-G-A

180615690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33867922-A-G

180615914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868074-G-A

180615918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868078-A-G

180616054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868214-T-C

180616197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868298-A-G

180616206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868307-G-A

180616206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868307-G-T

180616218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868315-G-A

180616218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868315-G-T

180616273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33868331-C-T

180616282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 33868343-T-C

180616361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 33868413-A-T

180616375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868427-T-G

180616429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868465-A-G

180616487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868473-G-T

180616494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868480-T-G

180616499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868485-A-G

180616541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33868527-A-G

180616739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868720-A-G

180616739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868720-A-T

180616952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33868930-T-C

180616974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33868955-A-G

180616989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868970-T-A

180616989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868970-T-C

180617014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33868996-T-G

180619093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869433-T-G

180619133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869465-A-G

180619164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869477-T-C

http://identifiers.org/hco/3/GRCh38#180619179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33869492-A-C

180619182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869495-G-A

180619182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869495-G-T

180619209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869512-T-C

180619231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869534-T-A

180619233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869536-T-C

180619238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33869541-A-G

180619409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33869700-G-A

180619409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33869700-G-T

180619471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33869759-T-C

180619683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33869940-A-G

http://identifiers.org/hco/3/GRCh38#180619691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33869948-A-C

180619691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33869948-A-T

http://identifiers.org/hco/3/GRCh38#180619807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33870057-A-C

180619807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870057-A-G

180619863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33870113-C-T

180619973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33870223-A-G

180619992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870236-T-C

180620011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870246-A-T

180620024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870259-A-T

180620029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870264-T-A

180620029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870264-T-C

180620070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870292-A-G

180620070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870292-A-T

180620113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33870336-T-A

180631409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33870918-G-T

180631499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33871007-C-T

180631644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33871317-A-G

180631841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33871413-G-T

180631858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33871430-C-T

180632567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33872084-C-T

180640877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33872549-G-A

180641070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33872695-T-A

180641297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33872891-A-G

180641297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33872891-A-T

180641365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873044-A-G

180641466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873151-T-C

180641557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873234-A-G

180641893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873841-G-A

180641893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873841-G-C

180641893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873841-G-T

180641974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33873932-T-A

180641999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33873963-T-A

http://identifiers.org/hco/3/GRCh38#180642003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#33873967-C-A

http://identifiers.org/hco/3/GRCh38#180642004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33873968-C-A

http://identifiers.org/hco/3/GRCh38#180642018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33873982-C-A

180642018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33873982-C-T

180642287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33874259-T-G

180642327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33874295-A-G

http://identifiers.org/hco/3/GRCh38#180642732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33874578-A-C

180642733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33874579-A-G

http://identifiers.org/hco/3/GRCh38#180642954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33874781-C-A

http://identifiers.org/hco/3/GRCh38#180643329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33874833-A-C

180643868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33875284-T-C

180644029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33875440-T-C

180644116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33875522-G-A

180644116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33875522-G-T

180644168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33875574-G-A

http://identifiers.org/hco/3/GRCh38#180644234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33875640-C-A

180644234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33875640-C-T

180644285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33875685-T-G

180644290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33875690-G-A

180644290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33875690-G-T

180645204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33877627-C-T

http://identifiers.org/hco/3/GRCh38#180645381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33877775-C-A

180645652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33878087-T-C

180646310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33878832-T-G

180646427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33878955-C-G

180646519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33879049-G-A

180646544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33879067-A-G

180646792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33879292-T-C

180646858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33879356-A-G

180646962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33879444-T-C

http://identifiers.org/hco/3/GRCh38#180646989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33879470-C-A

180646989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33879470-C-T

http://identifiers.org/hco/3/GRCh38#180646991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33879472-C-A

http://identifiers.org/hco/3/GRCh38#180647251-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33879713-A-C

http://identifiers.org/hco/3/GRCh38#180647275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33879740-A-C

180647275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33879740-A-G

180647288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33879755-G-A

180647288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33879755-G-T

180647601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880049-A-G

180647606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880054-T-C

180647839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880298-A-G

180647864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880310-C-T

180648001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880440-G-C

http://identifiers.org/hco/3/GRCh38#180648023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33880462-C-A

180648052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880491-T-A

180648052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880491-T-C

180648067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880505-A-G

180648095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880533-A-G

180648294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33880733-A-T

180648351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33880790-A-G

180648351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33880790-A-T

180648376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880822-T-C

180648410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880856-G-A

180648410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880856-G-T

180648422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33880868-A-G

http://identifiers.org/hco/3/GRCh38#180648457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33880897-C-A

180648719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33881109-T-C

http://identifiers.org/hco/3/GRCh38#180648847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33881209-C-A

180648847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33881209-C-T

180649495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33881830-A-G

180649939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33883500-A-G

180650406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33883935-A-G

180651298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884075-G-C

180651311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884086-G-C

180651311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884086-G-T

180651340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884114-T-C

180651365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884139-T-C

http://identifiers.org/hco/3/GRCh38#180651406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33884179-C-A

180651406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33884179-C-T

180651431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33884204-A-G

180651491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33884264-T-C

180651586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884359-T-C

180651689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884433-T-C

http://identifiers.org/hco/3/GRCh38#180651765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33884510-C-A

180651765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884510-C-T

http://identifiers.org/hco/3/GRCh38#180651861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33884537-C-A

180651896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884545-G-A

http://identifiers.org/hco/3/GRCh38#180651897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33884546-C-A

180651897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884546-C-T

180651955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884582-T-A

180651969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884593-G-A

180651969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884593-G-C

http://identifiers.org/hco/3/GRCh38#180652010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33884653-C-A

180652010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884653-C-T

180652106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33884742-A-G

180652381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33885025-A-G

180654733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33886652-A-G

http://identifiers.org/hco/3/GRCh38#180654734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33886653-C-A

180654734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33886653-C-T

180654752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33886667-G-T

180654792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33886707-A-G

180654792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33886707-A-T

180654855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33886770-A-G

http://identifiers.org/hco/3/GRCh38#180654876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33886791-C-A

180654876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33886791-C-T

180654941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33886856-T-C

http://identifiers.org/hco/3/GRCh38#180655137-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33887185-A-C

http://identifiers.org/hco/3/GRCh38#180655311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33887368-A-C

180655502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33887693-A-G

180655843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33889061-T-G

180658894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33890166-T-G

http://identifiers.org/hco/3/GRCh38#180659325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33890546-C-A

http://identifiers.org/hco/3/GRCh38#180659336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33890557-A-C

180659404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33890823-A-G

http://identifiers.org/hco/3/GRCh38#180659431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33890847-A-C

180659605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891018-T-C

180659610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891023-G-A

180659610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891023-G-C

http://identifiers.org/hco/3/GRCh38#180659662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33891075-C-A

180659662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891075-C-T

180659746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33891158-T-A

180659746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33891158-T-C

180659810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891222-T-C

180659990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891391-T-C

180660176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891595-T-A

180660294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891711-T-C

180660397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33891792-T-C

180660645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33892030-T-G

http://identifiers.org/hco/3/GRCh38#180660694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33892079-C-A

180660694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33892079-C-T

180660819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33892200-G-A

180660819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33892200-G-T

180660844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33892221-G-A

180660844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33892221-G-T

180660878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33892255-T-C

180661248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33892602-A-G

180661772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33893179-C-T

180661999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33893365-G-A

180662165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33893516-T-G

180662230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33893582-A-T

180662459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33893810-C-T

180662842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894182-C-T

180663499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894789-C-T

180663567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894874-G-C

180663575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894882-C-T

180663626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894943-C-T

180663634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894951-T-A

180663634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33894951-T-C

http://identifiers.org/hco/3/GRCh38#180663664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33895022-C-A

180663826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33895192-T-C

180663857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33895208-G-C

180664136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33895448-A-G

180678748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33897664-C-G

http://identifiers.org/hco/3/GRCh38#180679167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33897988-A-C

180679167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33897988-A-G

180679167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33897988-A-T

180679168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33897989-G-A

180679168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33897989-G-T

http://identifiers.org/hco/3/GRCh38#180679232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#33898093-C-A

180679232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33898093-C-T

http://identifiers.org/hco/3/GRCh38#180679400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33898363-A-C

http://identifiers.org/hco/3/GRCh38#180679463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33898417-C-A

180679463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 33898417-C-T

http://identifiers.org/hco/3/GRCh38#180679576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#33898517-C-A

180679576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33898517-C-G

180679576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33898517-C-T

180679606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25244
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 33898544-A-G