169511971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164050765-T-C

169512684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164049140-C-T

169512685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164049139-A-G

http://identifiers.org/hco/1/GRCh38#169512701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164049123-A-C

169513198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164048474-G-A

169513198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164048474-G-C

169513334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164048320-A-G

169513765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164047903-C-T

http://identifiers.org/hco/1/GRCh38#169514052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164047367-A-C

169514052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164047367-A-G

169514099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164047321-T-G

169514148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164047268-G-A

169514148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3 prime UTR variant
orthologous variants: 164047268-G-T

169514188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 164047234-C-T

http://identifiers.org/hco/1/GRCh38#169514247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164047182-C-A

169514247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 164047182-C-T

http://identifiers.org/hco/1/GRCh38#169514248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164047181-A-C

169514248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 164047181-A-G

169514272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 164047158-G-T

http://identifiers.org/hco/1/GRCh38#169514332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164047072-A-C

169514350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 164047054-G-A

169514367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 164047037-T-C

169514496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164046904-A-T

169515295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164045266-T-G

169515302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164045259-G-T

http://identifiers.org/hco/1/GRCh38#169515311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164045250-C-A

169515311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164045250-C-T

http://identifiers.org/hco/1/GRCh38#169515335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164045216-C-A

169515335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164045216-C-T

169515374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164045193-G-T

169515393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 164045173-A-T

169515482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 164045078-A-G

169515562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 164044998-A-G

169515628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: non_coding_transcript_exon_variant, splice_acceptor_variant
orthologous variants: 164044932-T-C

169515631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 164044929-G-A

http://identifiers.org/hco/1/GRCh38#169515646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164044905-A-C

169515651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 164044900-G-T

169515706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 164044796-G-T

http://identifiers.org/hco/1/GRCh38#169515806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164044494-A-C

169515812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044488-T-A

169515813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044487-A-G

169515874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044426-G-A

169515874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044426-G-T

169515891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044409-A-G

169515917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044381-T-C

169516409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044074-T-C

169516434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164044053-T-C

169516523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043980-A-G

169516630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043889-A-G

169516778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043756-C-G

169516890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043643-G-A

169516890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043643-G-T

http://identifiers.org/hco/1/GRCh38#169516921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164043611-A-C

169516949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043586-G-T

169517006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043530-A-G

169517056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043483-T-C

http://identifiers.org/hco/1/GRCh38#169517129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164043416-C-A

169517358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043206-A-G

169517373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043189-A-G

169517427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164043162-T-C

169517578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, undefined
orthologous variants: 164042967-C-T

169517899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042714-A-T

169518079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042408-G-C

169518170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042321-T-C

169518213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042280-T-C

169518308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042196-G-C

169518318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042186-C-T

169518364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042140-C-T

169518403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164042102-A-G

169518425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164042080-G-C

169518443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164042062-G-A

169518443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164042062-G-C

169518485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164042020-C-G

169518485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: 164042020-C-T

169518520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164041985-G-A

169518527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164041978-A-G

169518539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164041966-T-G

169518566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164041939-A-T

http://identifiers.org/hco/1/GRCh38#169518582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164041923-C-A

169518582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041923-C-T

169518635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041867-G-A

169518635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041867-G-T

169518731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041784-T-C

169518753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041762-T-C

169518990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041084-A-G

169519044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164041028-G-C

169519113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040967-G-A

169519458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040601-T-C

169519499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040560-A-G

169519556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040493-T-C

169519616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040433-C-T

169519707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040362-C-T

169519845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040238-G-C

169519852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164040231-A-G

169519955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039960-G-A

169520004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039908-T-A

169520037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039881-T-C

169520347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039629-T-C

169520379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039591-G-T

http://identifiers.org/hco/1/GRCh38#169520466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164039511-C-A

169520491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039487-T-G

169520512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164039467-T-C

169520672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164039307-A-T

169520771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164039213-C-G

169521142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038910-A-G

169521345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038757-C-T

169521511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038595-A-G

169521871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038510-G-A

169522039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038371-G-A

169522128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038276-C-T

http://identifiers.org/hco/1/GRCh38#169522250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164038150-A-C

169522306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038100-C-G

169522332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164038051-G-A

169522482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037895-A-G

169522599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037744-G-C

169522704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037636-G-A

169522859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037481-C-T

169523063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037302-G-T

169523102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037259-G-T

169523133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037242-T-C

169523149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037226-A-G

169523166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164037216-T-C

169523300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164037082-T-C

http://identifiers.org/hco/1/GRCh38#169523424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164036958-C-A

169523424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036958-C-T

169523484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036903-G-T

169523588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036799-G-C

169523644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036748-T-G

169523651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036741-A-T

169523666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036727-T-A

169523688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036706-G-T

169523705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036689-T-C

169523752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036656-T-G

169523764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036644-C-G

169523764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036644-C-T

169523785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036623-G-A

169523785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036623-G-C

169523785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036623-G-T

169523983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036302-G-A

169523983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036302-G-T

169523993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036292-T-A

169523993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036292-T-C

http://identifiers.org/hco/1/GRCh38#169523994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164036291-C-A

169523994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036291-C-T

169524038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036249-C-T

169524100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164036188-C-T

169524371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035945-G-A

169524422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035895-C-T

169524474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035847-G-A

169524512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035809-T-A

169524626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035695-A-G

169524711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035612-T-C

169524711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035612-T-G

169524719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035604-G-T

169524750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035573-A-T

169524769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035556-G-T

169524789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035536-G-A

169524803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035524-G-A

169524803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035524-G-T

169524806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035521-A-G

169524933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035398-A-G

169524933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035398-A-T

169524953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035378-A-G

169525296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035137-A-T

http://identifiers.org/hco/1/GRCh38#169525482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164035037-C-A

169525482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164035037-C-G

169525635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034933-T-C

http://identifiers.org/hco/1/GRCh38#169525674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164034894-A-C

169525766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034798-A-G

169525788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034796-G-T

http://identifiers.org/hco/1/GRCh38#169525789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164034795-C-A

169525789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034795-C-G

169525794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034790-G-A

169525794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034790-G-T

169525855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034732-T-C

169525867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034720-T-A

http://identifiers.org/hco/1/GRCh38#169525869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164034718-C-A

169525874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034717-C-T

169525966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164034628-A-G

169526046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034544-G-T

169526102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034490-C-T

http://identifiers.org/hco/1/GRCh38#169526105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164034487-C-A

169526107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034485-T-C

169526195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164034150-T-C

169526413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033967-A-G

169526413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033967-A-T

169526712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033681-G-A

169526712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033681-G-C

http://identifiers.org/hco/1/GRCh38#169526917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164033507-C-A

169527038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033358-C-T

169527199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033270-T-G

169527219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033245-G-A

169527249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033221-C-T

169527269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033201-T-C

169527275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164033195-G-A

http://identifiers.org/hco/1/GRCh38#169527781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164032665-C-A

169527781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164032665-C-T

http://identifiers.org/hco/1/GRCh38#169527800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164032651-C-A

169527800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164032651-C-T

http://identifiers.org/hco/1/GRCh38#169528118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164032325-C-A

169528216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164032239-T-G

169528390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164032080-G-A

169528390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164032080-G-C

169528450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164032026-G-A

169528942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164031376-G-T

169528952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164031366-A-G

169528965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164031353-T-C

169529173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029716-G-T

169529241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029649-A-G

169529319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029574-T-C

http://identifiers.org/hco/1/GRCh38#169529341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164029552-A-C

169529341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029552-A-G

169529347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029546-T-C

169529443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029467-G-A

169529502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029404-G-A

169529502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029404-G-T

169529573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029333-A-T

169529615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164029289-C-G

169529621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164029283-G-A

169529651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: 164029253-C-T

169529835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164029069-A-G

169529933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164028960-A-G

169529936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164028957-A-T

169529940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164028953-T-C

169530082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164028884-T-C

169530202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164028760-G-T

http://identifiers.org/hco/1/GRCh38#169530658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164026812-C-A

169530658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164026812-C-T

169530946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164026355-C-T

169531026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164026275-G-T

169531095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164026195-A-T

169531148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164026130-C-T

169531165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164026113-A-G

169531165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164026113-A-T

169536686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164023112-A-G

169536715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164023080-A-G

169536726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164023069-T-A

169536726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164023069-T-C

169536726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164023069-T-G

169540127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164022353-G-T

169540227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164022266-T-C

169540230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164022263-T-C

169540241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164022252-T-C

169540320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164022174-G-A

169540387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164022107-G-A

169540495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021999-T-C

169540522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021972-A-G

169540568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021926-T-C

169540880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021638-G-A

169540880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021638-G-C

169541154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021376-A-G

169541156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021374-G-C

http://identifiers.org/hco/1/GRCh38#169541170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164021360-A-C

169541176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021354-G-A

169541176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021354-G-T

169541208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021322-G-C

169541208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021322-G-T

169541212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021318-T-A

169541212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021318-T-G

169541229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021301-T-C

169541231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021299-G-A

169541266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021264-G-A

169541266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021264-G-C

169541266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021264-G-T

169541275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021255-C-T

169541292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021238-G-C

169541316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021214-G-A

169541316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021214-G-C

169541338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021192-A-G

169541338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: 164021192-A-T

169541346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021184-G-A

169541346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164021184-G-T

169541351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021179-T-C

169541353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021177-T-C

169541386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021144-A-G

169541392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021138-G-A

169541399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021131-T-C

169541399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164021131-T-G

169541637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020923-T-C

169541716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164020844-T-C

169541721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020839-T-C

169541721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020839-T-G

169541910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020653-T-C

169541928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164020635-T-G

169542150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020410-A-G

http://identifiers.org/hco/1/GRCh38#169542175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164020379-A-C

169542231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020323-T-C

169542411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164020197-G-T

http://identifiers.org/hco/1/GRCh38#169542419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164020189-C-A

http://identifiers.org/hco/1/GRCh38#169542509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#164020099-C-A

169542509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164020099-C-T

169542552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164020056-C-T

169542681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164019924-G-A

169542918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164019693-A-G

169542918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: 164019693-A-T

http://identifiers.org/hco/1/GRCh38#169543008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164019603-C-A

169543008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164019603-C-T

169543018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164019593-T-G

http://identifiers.org/hco/1/GRCh38#169543215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164019397-C-A

169543227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164019385-A-G

http://identifiers.org/hco/1/GRCh38#169543242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164019370-C-A

169543242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164019370-C-T

169543307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164019307-G-A

169543330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164019289-T-C

http://identifiers.org/hco/1/GRCh38#169543657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164018944-C-A

169543892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164018723-C-T

169544207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017976-G-A

169544207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017976-G-T

169544219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017964-T-A

169544219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017964-T-C

169544221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017962-G-T

http://identifiers.org/hco/1/GRCh38#169544229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164017955-C-A

169544229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017955-C-T

http://identifiers.org/hco/1/GRCh38#169544258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164017925-A-C

169544259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017924-G-A

169544259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017924-G-C

169544259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017924-G-T

169544278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017909-G-A

169544278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017909-G-T

http://identifiers.org/hco/1/GRCh38#169544574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164017615-C-A

169544602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017594-G-A

169544602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017594-G-T

169544642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017554-T-A

169544642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017554-T-C

http://identifiers.org/hco/1/GRCh38#169544901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164017325-C-A

169545124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164017101-A-G

169546391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014520-T-G

169546396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014515-C-T

169546555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, undefined
orthologous variants: 164014371-A-G

169546576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, undefined
orthologous variants: 164014350-T-C

169548505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014225-C-T

169548507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014223-G-A

169548529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014201-A-T

169548913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014137-T-C

169548968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014096-T-G

169548997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164014067-A-G

169549062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164013999-C-T

169549119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164013955-A-G

169549238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164013240-A-G

169549425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164013076-G-C

169549579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012931-T-C

169549579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012931-T-G

169549653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012851-A-G

169549750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012759-G-T

169549808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164012683-C-T

169549867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164012624-G-A

169549867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 164012624-G-T

169549868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164012623-A-G

169549919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164012572-G-C

169550588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, undefined
orthologous variants: 164012221-G-A

169550589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, undefined
orthologous variants: 164012220-C-T

169550659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous_variant, undefined
orthologous variants: 164012155-G-T

169550684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164012130-G-T

169550799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012008-G-A

169550799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012008-G-C

169550799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164012008-G-T

http://identifiers.org/hco/1/GRCh38#169550802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164012005-A-C

http://identifiers.org/hco/1/GRCh38#169550881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164011919-C-A

169551014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011870-T-C

169551064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011821-T-C

169551068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011817-G-T

169551727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011486-C-G

169551727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011486-C-T

169551747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011468-G-A

169551922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164011139-G-A

http://identifiers.org/hco/1/GRCh38#169552426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164010686-A-C

169552499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010619-T-C

169552529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010588-C-G

169552564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164010554-G-A

http://identifiers.org/hco/1/GRCh38#169552738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164010380-A-C

http://identifiers.org/hco/1/GRCh38#169552745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164010373-A-C

169552745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010373-A-G

169552787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010315-T-C

169552805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010297-G-A

169552805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010297-G-T

169552806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010296-T-G

http://identifiers.org/hco/1/GRCh38#169552847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164010263-C-A

169552847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010263-C-T

169554414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164010089-T-C

169554615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009883-A-G

169554660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009838-T-C

http://identifiers.org/hco/1/GRCh38#169554684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164009813-C-A

169554998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009533-A-G

169555014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009517-T-C

169555037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009494-G-T

http://identifiers.org/hco/1/GRCh38#169555075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164009456-C-A

169555075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009456-C-T

169555080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009451-G-A

169555086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009446-T-C

169555170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009353-C-G

169555194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164009332-G-A

169555251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: 164009275-C-T

169555281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164009245-G-T

169555329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164009197-A-G

169555359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009167-C-T

169555393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164009133-T-G

169555575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008962-G-A

169555592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008945-T-G

169555715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008740-A-G

169555847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008625-G-A

169555968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008515-A-G

169556053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008428-C-T

169556064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008417-T-G

169556159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008150-A-G

169556159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164008150-A-T

169556415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007891-T-G

169556420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007886-T-C

http://identifiers.org/hco/1/GRCh38#169556503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164007811-A-C

169556503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007811-A-G

169556503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007811-A-T

169556536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007780-G-T

169556553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007764-G-A

169556553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007764-G-T

169556613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007706-T-C

http://identifiers.org/hco/1/GRCh38#169556630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164007690-C-A

169556630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164007690-C-T

169556723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164007067-G-A

169556738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164007052-G-A

169556738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164007052-G-T

169556978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006862-T-A

169556978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006862-T-C

169556978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006862-T-G

169557136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006728-A-T

169557145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006719-T-C

169557146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006718-A-G

169557200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006655-G-C

169557231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006624-A-G

http://identifiers.org/hco/1/GRCh38#169557249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164006608-A-C

169557251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006606-G-A

169557315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006547-C-T

169557407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006461-T-G

169557525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006374-C-G

169557577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006310-A-G

169557806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164006099-G-C

169558363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164005561-C-T

169559035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164004047-T-A

169559035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164004047-T-G

http://identifiers.org/hco/1/GRCh38#169559053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164004029-C-A

169559099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164003987-G-A

169559099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164003987-G-T

http://identifiers.org/hco/1/GRCh38#169559138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164003946-C-A

169559310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164003774-G-A

169559800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164003327-T-C

169559933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164003222-G-A

169559951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164003205-G-T

169560134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164002278-T-C

169560145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164002267-C-G

169560185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164002224-G-A

http://identifiers.org/hco/1/GRCh38#169560474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#164001959-C-A

169560474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001959-C-T

169560486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001947-G-A

169560486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001947-G-C

169560486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001947-G-T

169560489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001944-C-T

169560697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 164001736-T-C

169560774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 164001659-A-T

169560781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001652-G-A

169560849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001599-G-A

169560849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001599-G-T

169560867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001581-G-A

169560867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001581-G-T

169560927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001526-A-G

169561338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164001104-G-A

169561682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164000798-C-T

169561864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164000686-T-C

169561913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164000638-C-T

169561981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164000592-T-C

169562017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 164000556-T-C

169564773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999597-A-G

169564783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999587-T-G

http://identifiers.org/hco/1/GRCh38#169564806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163999564-A-C

169564812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999558-G-A

169564828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999539-A-G

169564864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999499-T-C

169564911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999443-T-C

169565333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999037-T-A

169565344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163999026-T-A

169565407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163998963-T-C

http://identifiers.org/hco/1/GRCh38#169565686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163998738-A-C

169566088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163998328-G-A

169566229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163998196-A-G

169566265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163998160-T-C

http://identifiers.org/hco/1/GRCh38#169566301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163998124-A-C

169566733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163997427-T-C

169566918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163997154-T-C

169567588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996714-A-G

169567588-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996714-A-T

169567662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996646-C-T

169567814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996551-G-C

169567841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996528-A-G

169568013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996373-A-G

169568085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996316-A-G

169568276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163996153-G-C

169568660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163995779-G-C

169569049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163995403-G-A

169569111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163995342-T-C

169569218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163995247-G-A

169569221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163995244-A-G

http://identifiers.org/hco/1/GRCh38#169569643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163991175-C-A

169569643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163991175-C-T

169569762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163991065-T-C

169569801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163991027-C-T

169569929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163990906-G-T

http://identifiers.org/hco/1/GRCh38#169570023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163990823-A-C

169570084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163990757-A-G

169570100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, undefined
orthologous variants: 163990741-C-T

169570168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron_variant, undefined
orthologous variants: 163990670-G-A

169570308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163990529-C-G

169570493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163990375-A-T

169571905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989786-C-T

169571964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989731-G-A

169571973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989715-G-A

169572029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989660-T-A

http://identifiers.org/hco/1/GRCh38#169572129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163989557-A-C

169572433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989259-A-G

http://identifiers.org/hco/1/GRCh38#169572471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163989221-C-A

169572471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989221-C-G

169572582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163989122-G-C

169574819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988996-C-T

169574895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988905-A-G

169574989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988825-C-T

169575040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988765-A-G

169575243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988562-A-G

169575277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988526-G-A

169575351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988460-C-T

169575355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988456-C-T

http://identifiers.org/hco/1/GRCh38#169575455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163988359-C-A

169575771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988061-G-A

169575827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163988012-C-T

169575896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987958-G-C

169575896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987958-G-T

169575901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987953-T-G

169575919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987932-G-T

169576169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987689-C-T

169576500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987109-G-A

169576549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987060-G-T

169576565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163987044-C-T

http://identifiers.org/hco/1/GRCh38#169576629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163986984-A-C

http://identifiers.org/hco/1/GRCh38#169576670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163986934-A-C

169576670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163986934-A-T

169576700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163986905-T-C

169577115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163986524-C-G

169577149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163986490-A-G

http://identifiers.org/hco/1/GRCh38#169577812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163986232-A-C

http://identifiers.org/hco/1/GRCh38#169577890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163986147-C-A

169577890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163986147-C-T

169578298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163985831-T-C

169578298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163985831-T-G

169578322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163985809-C-T

169578488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163985641-G-A

169578573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163985556-C-T

169578787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163985450-A-G

169579331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163984997-C-T

http://identifiers.org/hco/1/GRCh38#169579369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163984959-C-A

169579369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163984959-C-T

169579390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163984938-T-C

169579425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163984900-T-G

169579698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163984600-C-T

169580918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983571-C-G

169580918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983571-C-T

169580919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983570-T-A

169580959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983539-G-A

169581052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983446-G-A

169581101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983397-A-G

http://identifiers.org/hco/1/GRCh38#169581102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163983396-C-A

169581319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983285-C-T

169581342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983274-G-A

169581355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983258-G-T

169581582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983183-G-A

169581662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163983114-G-T

169582027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163982781-A-G

169582073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163982735-A-G

169582073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163982735-A-T

169582256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163982561-G-A

169582257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163982560-G-T

169582469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 163981943-G-A

169582469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 163981943-G-T

169582571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163981846-T-A

169582863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163981552-T-C

169583045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163981354-T-C

169583059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163981340-T-A

169583060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163981339-A-T

169585102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980896-G-A

169585103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980895-G-T

http://identifiers.org/hco/1/GRCh38#169585261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163980737-A-C

169585261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980737-A-G

169585289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980704-C-T

169585408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980561-A-G

169585415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980549-T-G

169585537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980441-T-A

169585617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980310-G-A

169585814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980113-A-G

169585845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980070-A-G

169585852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980063-A-G

169585896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163980025-G-A

169586064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: intron variant
orthologous variants: 163979862-T-C

http://identifiers.org/hco/1/GRCh38#169586245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#163979671-C-A

169586245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 163979671-C-G

169586296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, undefined
orthologous variants: 163979620-G-C

169586296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense_variant, undefined
orthologous variants: 163979620-G-T

169586328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 163979588-C-G

169586340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 163979576-G-A

169586340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: missense variant
orthologous variants: 163979576-G-C

169586342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous variant
orthologous variants: 163979574-G-T

169586366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous_variant, undefined
orthologous variants: 163979550-G-A

169586366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: synonymous_variant, undefined
orthologous variants: 163979550-G-C

169586467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 5 prime UTR variant
orthologous variants: 163979465-T-A

169586467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 5 prime UTR variant
orthologous variants: 163979465-T-C

169586468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 5 prime UTR variant
orthologous variants: 163979464-G-A

169586468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 5 prime UTR variant
orthologous variants: 163979464-G-T

http://identifiers.org/hco/1/GRCh38#169586550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3542
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#163979395-C-A