http://identifiers.org/hco/5/GRCh38#151504181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55141531-C-A

151504181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141531-C-T

151504206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141542-T-C

151504210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141546-G-A

151504210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141546-G-T

http://identifiers.org/hco/5/GRCh38#151504213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55141549-C-A

http://identifiers.org/hco/5/GRCh38#151504520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55141822-C-A

151504520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141822-C-T

151504548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141851-G-A

151504581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141884-T-C

151504591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141894-C-T

151504599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141902-A-G

http://identifiers.org/hco/5/GRCh38#151504642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55141944-A-C

151504642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55141944-A-G

151504725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142024-C-T

151504831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142114-T-C

http://identifiers.org/hco/5/GRCh38#151504881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142141-C-A

151504881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142141-C-T

http://identifiers.org/hco/5/GRCh38#151504925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142166-C-A

151504925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142166-C-T

151504975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142221-G-A

151504975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142221-G-T

151504991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142232-A-G

151504992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142233-G-A

151504992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142233-G-C

151505038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142279-A-T

151505045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142286-T-C

http://identifiers.org/hco/5/GRCh38#151505050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142294-C-A

151505050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142294-C-T

http://identifiers.org/hco/5/GRCh38#151505069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142313-C-A

http://identifiers.org/hco/5/GRCh38#151505095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142340-C-A

151505096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142341-A-G

151505102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142347-C-G

151505140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142396-T-A

151505140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142396-T-C

http://identifiers.org/hco/5/GRCh38#151505224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142474-A-C

151505224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142474-A-G

http://identifiers.org/hco/5/GRCh38#151505256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142508-A-C

151505256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142508-A-G

151505256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142508-A-T

http://identifiers.org/hco/5/GRCh38#151505343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142572-C-A

151505343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142572-C-G

151505343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142572-C-T

151505411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142640-G-A

151505411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142640-G-C

151505411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142640-G-T

151505457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142693-T-C

151505457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142693-T-G

http://identifiers.org/hco/5/GRCh38#151505476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55142710-C-A

151505523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142750-C-G

151505523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142750-C-T

151505553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 55142780-G-A

151505651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, stop_gained
orthologous variants: 55142878-G-A

151505808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55143035-A-G

151505968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55143195-A-G

151505968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55143195-A-T

http://identifiers.org/hco/5/GRCh38#151506054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55143281-C-A

151506054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55143281-C-T

151506171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143398-A-G

151506204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143437-G-A

151506204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143437-G-T

151506227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143461-G-C

151506227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143461-G-T

151506245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143479-A-G

151506314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143545-G-C

151506342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143571-A-G

151506510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143725-G-T

151506653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55143844-C-T

http://identifiers.org/hco/5/GRCh38#151506938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55144102-C-A

151506953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55144119-A-T

http://identifiers.org/hco/5/GRCh38#151507035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55144224-C-A

151507035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55144224-C-T

http://identifiers.org/hco/5/GRCh38#151507078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55144274-C-A

151507078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55144274-C-T

http://identifiers.org/hco/5/GRCh38#151509937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55146840-C-A

151509937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55146840-C-T

151510003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55146915-G-A

151510012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55146921-T-C

151510275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55147172-A-G

151510275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55147172-A-T

151510285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55147188-T-A

151512205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55147370-T-A

151512324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55147489-C-T

151512351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, stop_gained
orthologous variants: 55147516-G-A

151512553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55147718-T-G

151514437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55148995-T-A

151514464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149016-C-T

151514490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149029-C-T

http://identifiers.org/hco/5/GRCh38#151514496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55149035-C-A

151514500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149039-A-T

151514529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149053-G-A

151514646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149152-G-C

151514664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149170-G-A

151514886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149314-G-A

151514980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149366-T-G

151515226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149544-C-G

151515261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149585-A-G

151515660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55149926-A-G

151515927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55150174-A-G

151516022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55150275-C-T

151517438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151107-G-A

151517723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55151375-C-G

151517734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55151386-A-G

151517786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151437-G-C

151517786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151437-G-T

151517851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151497-G-A

151517851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151497-G-T

151517860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151506-A-T

151518083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55151727-C-T

151520687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152390-A-G

151520699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152402-G-A

151520699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152402-G-C

151520921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152587-G-A

151520927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152593-A-G

151520995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152642-T-C

http://identifiers.org/hco/5/GRCh38#151521133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55152774-C-A

151521133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152774-C-T

151521215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55152843-T-C

151521286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55152898-G-A

151521670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55153282-C-G

151521713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55153325-A-G

151521739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153351-G-A

151521742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153354-C-G

151521742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153354-C-T

151521921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, stop_gained
orthologous variants: 55153533-G-A

151521921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55153533-G-C

151521976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153588-A-G

151522027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153639-T-C

151522032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55153644-C-G

151522032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55153644-C-T

151522033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153645-A-G

151522036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153648-G-C

http://identifiers.org/hco/5/GRCh38#151522048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55153660-C-A

151522048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55153660-C-T

151522150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153754-G-T

151522153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153756-G-A

151522153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153756-G-C

http://identifiers.org/hco/5/GRCh38#151522185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55153787-C-A

151522185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153787-C-T

151522210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153809-G-C

151522210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153809-G-T

151522286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153880-G-A

151522286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153880-G-T

151522296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153890-A-G

151522296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55153890-A-T

151522418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55154051-C-G

151522488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55154135-C-T

151522495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55154142-C-T

151525852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55156772-G-A

151525876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55156796-G-T

151525885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55156805-C-G

151525885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55156805-C-T

151525926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55156846-G-A

151525926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55156846-G-C

151526051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55156971-T-A

http://identifiers.org/hco/5/GRCh38#151526064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55156984-C-A

151526064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55156984-C-T

http://identifiers.org/hco/5/GRCh38#151526087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55157003-C-A

151526088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55157004-T-C

151526220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55157076-T-G

151527016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158208-T-C

151527083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158274-A-G

151527107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158315-C-T

151527186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158371-G-A

151527186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158371-G-T

151527326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55158495-G-A

http://identifiers.org/hco/5/GRCh38#151527384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55158553-C-A

151527405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158575-G-T

151527510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158632-G-A

151527510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158632-G-T

151527526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158646-T-G

151527542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158661-A-G

151527865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158904-T-C

151527865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158904-T-G

151527869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158908-A-G

151527869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55158908-A-T

151528185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159192-G-A

151528195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159202-G-T

151528198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159205-G-A

151528198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159205-G-T

151528449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159432-G-A

151528548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159532-G-A

151528548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159532-G-C

151528548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159532-G-T

151528718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55159700-G-T

151529107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160003-G-T

151529108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160004-G-T

151529145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160048-T-C

151529145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160048-T-G

151529203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55160105-G-A

151529203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55160105-G-C

151529203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55160105-G-T

151529241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55160143-G-A

151529250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55160152-C-T

151529322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55160224-G-A

151529415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160317-C-T

151530955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160358-G-A

151530961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160367-G-C

151531081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160468-G-C

151531275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160634-C-T

151531401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160748-A-G

151531441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160791-G-A

151531441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160791-G-T

151531530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160841-A-G

http://identifiers.org/hco/5/GRCh38#151531551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55160869-C-A

151531551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160869-C-G

151531551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160869-C-T

151531557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55160877-G-A

151531680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55161005-G-A

151531680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55161005-G-C

151531792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55161117-G-A

151531792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55161117-G-T

151531855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55161180-T-C

151531858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55161183-C-T

151531930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55161255-G-A

151531940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55161265-G-A

151531940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55161265-G-T

151531967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55161292-G-A

151532008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161330-C-T

151532052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161341-G-A

151532066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161355-G-A

151532066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161355-G-T

http://identifiers.org/hco/5/GRCh38#151532067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55161356-C-A

151532067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161356-C-G

151532067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161356-C-T

151532082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161369-A-G

151533495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55161900-C-T

http://identifiers.org/hco/5/GRCh38#151533547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55161943-C-A

151533843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55162158-T-C

151533900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55162215-A-G

151534315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55163719-T-C

151534332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55163735-A-G

http://identifiers.org/hco/5/GRCh38#151534333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55163736-C-A

151534333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55163736-C-T

151534467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55163879-G-A

151534503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55163915-C-G

151534503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55163915-C-T

151534537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55163949-G-C

151534537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55163949-G-T

http://identifiers.org/hco/5/GRCh38#151534554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55163966-C-A

151534554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 55163966-C-T

151534575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 55163987-C-T

151534669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164081-G-A

151534669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164081-G-T

151534708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164110-A-G

151534713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164115-T-C

151534980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164354-T-C

http://identifiers.org/hco/5/GRCh38#151535017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55164388-A-C

151535017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164388-A-T

http://identifiers.org/hco/5/GRCh38#151535021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55164392-A-C

151535029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164400-G-A

151535029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55164400-G-T

151536529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55165863-G-A

151536571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55165902-T-G

151536626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55165957-G-C

151536626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55165957-G-T

151537658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55166701-G-A

151537658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55166701-G-T

151537684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55166722-G-T

151537829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55166846-G-A

151537911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55166928-A-G

151538003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55167017-G-T

http://identifiers.org/hco/5/GRCh38#151538094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55167073-C-A

151538094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55167073-C-G

151538095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55167074-A-G

151538220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55167931-G-C

151538294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55167993-C-G

151538294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55167993-C-T

151538386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168077-G-A

151538517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168207-T-C

151538563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168252-A-G

151539037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168401-A-G

http://identifiers.org/hco/5/GRCh38#151539060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55168423-C-A

151539071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168434-C-G

151539071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168434-C-T

151539219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168568-T-C

151539262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant
orthologous variants: 55168608-G-A

151539313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168652-T-C

151539316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168655-A-G

151539435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168771-G-A

151539435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168771-G-T

151539458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168785-T-C

151539542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55168871-T-A

http://identifiers.org/hco/5/GRCh38#151539619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55168967-A-C

151540192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55169498-T-G

151540218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55169524-C-G

151540218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55169524-C-T

151540528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55169676-T-C

151540544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55169692-T-A

http://identifiers.org/hco/5/GRCh38#151540681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55169827-C-A

151540752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55169898-G-A

http://identifiers.org/hco/5/GRCh38#151540873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55170015-A-C

http://identifiers.org/hco/5/GRCh38#151540911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55170053-C-A

151540911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170053-C-T

151540959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170090-C-G

151541194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170369-G-A

151541194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170369-G-T

151541260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170392-G-C

151541300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170429-T-C

http://identifiers.org/hco/5/GRCh38#151541465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55170572-A-C

151541472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170579-C-T

151541543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170650-G-A

151541543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55170650-G-T

151542136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171746-G-A

151542136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171746-G-T

http://identifiers.org/hco/5/GRCh38#151542222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55171802-C-A

151542222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171802-C-T

151542226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171806-T-A

151542226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171806-T-C

151542235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171815-A-G

151542259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55171838-C-T

http://identifiers.org/hco/5/GRCh38#151542266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55171845-C-A

151542343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55171922-T-C

http://identifiers.org/hco/5/GRCh38#151542433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55172012-A-C

151542433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172012-A-G

151542433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55172012-A-T

151542691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172270-C-T

151542739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172318-T-C

http://identifiers.org/hco/5/GRCh38#151542796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55172375-C-A

151542796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172375-C-T

151542914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55172496-C-T

151543264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172849-G-C

151543318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172903-C-T

151543378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55172963-T-C

151543429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55173014-T-C

http://identifiers.org/hco/5/GRCh38#151543458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55173043-C-A

151543552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55173137-T-G

151543975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55173560-A-G

151544071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55173656-C-T

http://identifiers.org/hco/5/GRCh38#151544089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55173674-A-C

151544143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55173728-T-C

151544149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55173734-C-G

151544164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55173749-G-A

151544449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55174034-T-G

http://identifiers.org/hco/5/GRCh38#151544473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55174058-A-C

151544473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55174058-A-G

http://identifiers.org/hco/5/GRCh38#151544486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55174071-A-C

151544486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55174071-A-T

151544566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55174151-A-G

151544691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55174276-G-A

151544798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55174383-G-A

151544872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55174457-T-C

151545187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55174772-G-A

151545187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55174772-G-T

151545247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55174832-T-C

151545630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55175215-T-C

151545681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55175266-C-G

151545764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55175349-T-A

151545764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55175349-T-C

151545871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55175456-A-G

http://identifiers.org/hco/5/GRCh38#151545916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55175501-A-C

151546210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55175795-T-C

151546348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55175933-A-T

http://identifiers.org/hco/5/GRCh38#151546357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55175942-A-C

151546428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176015-A-G

151546439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176026-G-A

151546439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176026-G-T

151546568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176160-A-G

151549079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176516-G-A

151549157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176573-G-T

151549185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176601-G-T

151549234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176649-G-C

151549234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176649-G-T

151549286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176697-G-A

151549286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55176697-G-T

151549423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55176833-C-T

151549431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55176841-G-T

151549470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55176880-G-A

http://identifiers.org/hco/5/GRCh38#151549600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55177005-A-C

http://identifiers.org/hco/5/GRCh38#151549638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55177034-A-C

151549638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177034-A-G

151549710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177084-T-C

151549733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177107-T-C

151549868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177216-T-A

151550010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177578-T-C

151550109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177668-C-T

151550125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177684-G-A

151550176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177729-C-T

151550268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177820-T-C

http://identifiers.org/hco/5/GRCh38#151550444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55177992-C-A

151550444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55177992-C-T

151550465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55178013-T-A

151550480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55178138-G-A

151550480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55178138-G-T

151550539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55178356-C-G

http://identifiers.org/hco/5/GRCh38#151550617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55178508-C-A

151550617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55178508-C-G

151550617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55178508-C-T

151550629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55178520-G-A

151550737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55178628-C-T

151550945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55178839-C-T

http://identifiers.org/hco/5/GRCh38#151551016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55178903-C-A

151551016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55178903-C-T

151551268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55179847-A-G

http://identifiers.org/hco/5/GRCh38#151551424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55180001-C-A

http://identifiers.org/hco/5/GRCh38#151551431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55180008-C-A

151551533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55180110-G-T

151552079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55181653-G-A

151552348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55181747-T-A

http://identifiers.org/hco/5/GRCh38#151552362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55181765-C-A

151552362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55181765-C-T

151552377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55181780-G-A

151552556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55181963-T-C

151552647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182058-C-T

151552732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182166-A-G

151552929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182458-G-A

151552982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182534-C-T

151553033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182585-A-G

151553033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182585-A-T

151553049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182597-G-A

151553049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182597-G-T

151553071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182619-G-A

151553071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182619-G-C

151553087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182635-A-T

151553091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182639-G-A

151553091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182639-G-C

151553091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182639-G-T

151553123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182659-G-T

151553150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182685-C-T

151553153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182688-G-C

151553153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182688-G-T

151553280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55182803-C-T

151553528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182985-T-A

151553529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182986-G-T

151553540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55182997-G-A

151553641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55183095-T-A

151553641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55183095-T-C

151554350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55186888-C-T

151554377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55186915-C-T

151554656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55187194-A-G

151554708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187247-A-G

151554716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187254-A-G

151554791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187322-A-G

151554795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187326-T-A

151554795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187326-T-C

151554795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187326-T-G

151554940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187414-C-G

151555050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187470-T-C

151555078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55187495-A-G

151555645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188693-C-T

http://identifiers.org/hco/5/GRCh38#151555650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55188698-A-C

151555650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188698-A-T

151555858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55188880-G-A

151556099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189118-C-T

151556109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189128-G-A

151556115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189134-C-G

151556136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189155-C-T

151556158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189177-A-G

151556158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189177-A-T

151556254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189280-T-A

151556254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189280-T-C

151556265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189299-A-G

http://identifiers.org/hco/5/GRCh38#151556289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55189327-A-C

151556289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189327-A-G

http://identifiers.org/hco/5/GRCh38#151556308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55189343-C-A

151556349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55189389-G-A

151556349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55189389-G-C

http://identifiers.org/hco/5/GRCh38#151556480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55189519-C-A

151556480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189519-C-T

151557002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189639-G-A

151557021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189657-A-G

151557064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189700-C-G

151557113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189750-G-A

151559769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55189857-A-G

151559928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190010-C-G

151560023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190128-C-G

151560073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190175-T-C

151560109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55190210-C-T

151561871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55192731-T-A

151562511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55193299-G-A

151563001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194180-A-G

151563002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194181-T-C

151563425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55194564-T-C

151563425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55194564-T-G

151563498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55194637-G-A

151563510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55194649-G-A

151563510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55194649-G-T

151563676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194814-G-T

http://identifiers.org/hco/5/GRCh38#151563683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55194821-A-C

151563683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55194821-A-G

151563869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55195468-T-A

151565402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199541-T-G

151565455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199594-G-T

151565457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199596-G-C

151565459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199598-A-T

151565461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199600-A-G

151565466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199605-T-C

151565468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199607-T-C

151565477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199616-A-G

151565489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199635-A-G

http://identifiers.org/hco/5/GRCh38#151565556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55199750-C-A

151565556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199750-C-G

151565556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199750-C-T

151565577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199762-C-T

151565579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199764-G-A

151565579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199764-G-T

http://identifiers.org/hco/5/GRCh38#151565598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55199783-C-A

151565598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55199783-C-T

http://identifiers.org/hco/5/GRCh38#151565636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55199791-C-A

151565874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200015-C-T

151565886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200027-C-G

151565886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200027-C-T

151565915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200056-C-T

151566004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55200145-C-T

151566067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55200208-G-A

151566079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200220-A-T

151566393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200534-C-T

151566484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55200625-G-A

151566484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200625-G-C

151566625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55200766-T-G

151566658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55200799-A-G

http://identifiers.org/hco/5/GRCh38#151566669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55200810-C-A

151566669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55200810-C-T

http://identifiers.org/hco/5/GRCh38#151566682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55200823-C-A

151566682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55200823-C-G

151566883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201024-G-A

151566979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201120-G-A

151566979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201120-G-T

151567030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201171-G-C

http://identifiers.org/hco/5/GRCh38#151567116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#55201257-C-A

151567116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201257-C-G

151567116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201257-C-T

151567186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201327-C-G

151567186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201327-C-T

151567204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201345-G-A

151567204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201345-G-C

151567337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201478-C-T

151567366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201507-A-G

151567471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201612-A-G

151567588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201729-A-G

151567612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55201753-G-T

151567839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201980-C-G

151567839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55201980-C-T

151567865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55202006-T-C

151567897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202038-G-A

151567897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202038-G-T

151567964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55202105-A-G

151568119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202260-G-A

http://identifiers.org/hco/5/GRCh38#151568314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55202455-A-C

151568377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202518-A-G

151568440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55202581-C-G

151568440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202581-C-T

http://identifiers.org/hco/5/GRCh38#151568469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55202610-C-A

http://identifiers.org/hco/5/GRCh38#151568494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55202635-A-C

151568494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202635-A-G

151568502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202643-G-A

151568502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55202643-G-T

151568512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202653-G-A

151568512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55202653-G-T

151568539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55202680-C-G

151568569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202710-G-A

151568617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202758-A-T

http://identifiers.org/hco/5/GRCh38#151568821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55202962-A-C

151568821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55202962-A-G

151568906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55203047-G-A

151569589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203381-C-T

151569592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203384-G-A

151569592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203384-G-C

151569593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203385-T-C

151569701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203490-T-C

http://identifiers.org/hco/5/GRCh38#151569818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55203583-C-A

151569843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55203608-A-G

151570071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55204242-C-T

151570439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55204563-C-G

151570439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55204563-C-T

151570663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55204721-C-T

151570853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55204901-A-T

151571325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205336-C-T

151571934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55205931-C-T

151571980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55206013-C-G

151572006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55206043-T-G

151572105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55206102-A-G

151572259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55206237-T-C

151572622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55206815-A-T

151573039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207156-C-G

151573043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55207160-C-T

151574435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210381-G-T

151574681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210772-T-C

151574901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210976-G-A

151574920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55210996-G-A

151574990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211053-A-G

151575026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211087-A-G

151575032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55211093-G-A

151578507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55214844-G-A

151580416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217168-G-A

151580472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217226-T-A

151580472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55217226-T-C

151581029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218028-C-T

151581067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218062-G-A

151581275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218246-C-T

151581463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218398-C-T

151581514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218437-G-A

151581646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218545-T-C

151581874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55218927-C-G

http://identifiers.org/hco/5/GRCh38#151582324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55219271-A-C

151582594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219491-T-C

151582712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219588-G-A

151582986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219783-T-C

151583201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55219959-G-T

151583346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220072-A-G

151583420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220143-A-G

151583439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220215-A-G

151583577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55220347-G-A

151585864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221301-G-A

151585907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221322-G-T

http://identifiers.org/hco/5/GRCh38#151586034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55221440-A-C

151586183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55221577-A-T

151586298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221675-G-A

151586386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55221772-G-A

151586635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222006-C-G

151586944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222539-C-T

151587015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222634-G-A

151587015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222634-G-T

151587063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55222682-G-A

http://identifiers.org/hco/5/GRCh38#151587156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55222754-C-A

151587619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223170-C-G

151587761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223321-G-A

151587761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223321-G-T

151588143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223745-A-G

151588284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223897-A-G

151588393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55223992-G-T

151588404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224003-T-A

151588412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224011-G-T

151588442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55224041-G-A

151590133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226279-G-A

151590141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226287-C-T

151590199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226355-T-C

151590663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226827-C-G

151590663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226827-C-T

151590755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226920-C-T

151590815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226972-T-C

151590826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55226981-C-T

151590875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227014-T-C

151590912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227053-T-C

151591060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227186-A-T

151591102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227225-C-T

http://identifiers.org/hco/5/GRCh38#151591129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#55227252-C-A

151591129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227252-C-G

151591129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55227252-C-T

151591273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 55227394-C-T

151592881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55230523-G-T

151593046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55230629-G-C

151593082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55230663-G-A

151593124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55230703-T-C

151594206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3596
most severe consequence: intron variant
orthologous variants: 55231222-T-C