2269699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352347-C-G

2269699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352347-C-T

http://identifiers.org/hco/4/GRCh38#2269782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34352434-C-A

2269913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352551-G-A

2269913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352551-G-T

2269929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352567-G-A

2269949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352587-G-T

2269999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352615-C-G

2269999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352615-C-T

2270057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352670-T-G

2270091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352701-G-A

2270189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352798-G-A

http://identifiers.org/hco/4/GRCh38#2270231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34352843-C-A

2270231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352843-C-T

http://identifiers.org/hco/4/GRCh38#2270420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34352963-C-A

2270427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352973-G-A

2270427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34352973-G-T

2270468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34353015-G-A

2270468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34353015-G-C

2270468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34353015-G-T

http://identifiers.org/hco/4/GRCh38#2270632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34353180-C-A

2270632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34353180-C-T

2270679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 3 prime UTR variant
orthologous variants: 34353254-T-C

2270815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous variant
orthologous variants: 34353403-G-C

2270994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353585-T-C

2270994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353585-T-G

2270998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353589-G-A

2270998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353589-G-T

2270999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353590-A-G

http://identifiers.org/hco/4/GRCh38#2271116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34353730-C-A

2271116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353730-C-T

http://identifiers.org/hco/4/GRCh38#2271150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34353750-C-A

2271163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353763-A-G

2271163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34353763-A-T

2271433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34354043-C-G

2271433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34354043-C-T

http://identifiers.org/hco/4/GRCh38#2271557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34354413-C-A

2271748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34354899-C-T

http://identifiers.org/hco/4/GRCh38#2271883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34355025-C-A

2271883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34355025-C-T

2271902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34355046-G-A

2271902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34355046-G-T

2272023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34355175-G-C

2272424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34355589-G-A

2272430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34355595-G-A

2273383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356333-T-A

2273383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356333-T-C

http://identifiers.org/hco/4/GRCh38#2273439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34356357-C-A

2273440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356358-T-A

2273440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356358-T-C

2273440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356358-T-G

http://identifiers.org/hco/4/GRCh38#2273507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34356421-C-A

http://identifiers.org/hco/4/GRCh38#2273519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34356433-C-A

2273519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356433-C-T

2273578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356481-C-T

2273618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356517-C-T

2273646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356542-G-A

2273885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356788-C-T

2273951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356839-G-A

2273951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34356839-G-T

http://identifiers.org/hco/4/GRCh38#2273964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34356845-A-C

http://identifiers.org/hco/4/GRCh38#2273989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34356872-C-A

2273989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: 34356872-C-G

http://identifiers.org/hco/4/GRCh38#2274032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#34356913-A-C

2274078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous_variant, undefined
orthologous variants: 34356953-C-G

2274081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous_variant, undefined
orthologous variants: 34356956-G-A

2274207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 34357082-T-C

2274240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: 34357113-T-C

http://identifiers.org/hco/4/GRCh38#2280755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34362433-C-A

2286812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364216-G-T

2287072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364431-G-A

2287072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364431-G-T

http://identifiers.org/hco/4/GRCh38#2287108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34364458-C-A

2287108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364458-C-T

2287118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364468-A-G

2287118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364468-A-T

2287144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364482-G-A

2287144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364482-G-T

http://identifiers.org/hco/4/GRCh38#2287279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34364584-C-A

2287279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364584-C-T

2287313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364606-A-G

http://identifiers.org/hco/4/GRCh38#2287369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34364658-C-A

2287381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34364669-T-C

http://identifiers.org/hco/4/GRCh38#2287714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34365031-C-A

2290173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34366415-A-G

2290174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34366416-G-A

2291636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34367236-G-A

2291840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34367420-G-C

2291953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34367505-G-A

2291979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34367550-C-T

2291980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34367551-G-A

http://identifiers.org/hco/4/GRCh38#2292206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34367757-C-A

2300154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34369240-G-A

http://identifiers.org/hco/4/GRCh38#2300168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34369254-A-C

2300330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34369385-T-C

2300538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34369625-G-A

2301003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34370829-G-A

2301075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34370910-C-T

2301107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34370938-C-T

2301275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371084-C-T

2301276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371085-G-A

2301347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371147-C-T

2301458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371239-C-T

2301494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371286-T-C

2301569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371360-G-A

2301617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371378-G-A

http://identifiers.org/hco/4/GRCh38#2301983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34371732-C-A

2301983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371732-C-T

2302009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34371758-T-A

http://identifiers.org/hco/4/GRCh38#2302648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34372439-A-C

2302853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34372657-G-A

2303025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34372703-G-A

2303102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34372760-C-T

2303124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34372770-A-G

2303144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34372794-A-G

2303226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34372864-C-T

2303359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373024-C-G

2303399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373073-G-A

2303624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373351-C-T

2303649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373380-T-A

2303679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373391-C-T

2303864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373566-G-A

2303933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373593-C-T

http://identifiers.org/hco/4/GRCh38#2304011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34373656-C-A

2304011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373656-C-T

http://identifiers.org/hco/4/GRCh38#2304234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34373848-C-A

2304234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373848-C-T

2304244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373857-G-A

2304244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373857-G-C

2304253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373866-G-A

2304253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373866-G-C

2304253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373866-G-T

2304255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373870-A-G

2304255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34373870-A-T

http://identifiers.org/hco/4/GRCh38#2304363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34374012-C-A

2304363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374012-C-T

2304403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374052-G-A

2304403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374052-G-T

2304675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374342-C-T

2304816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374501-T-C

2304816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374501-T-G

2304828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374513-G-A

2304828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374513-G-C

2304828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374513-G-T

http://identifiers.org/hco/4/GRCh38#2304920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34374605-C-A

2304920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374605-C-G

2304920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374605-C-T

2304937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374622-G-A

2304937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374622-G-C

2305026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34374711-C-G

http://identifiers.org/hco/4/GRCh38#2305068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34374744-C-A

2305068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374744-C-T

2305110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34374786-T-G

http://identifiers.org/hco/4/GRCh38#2305158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34374831-A-C

2305332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34375005-C-T

2305443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34375116-G-A

2305443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34375116-G-T

2305467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34375140-G-A

2305467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 34375140-G-T

2305515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34375188-C-T

2305564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375232-G-A

2305564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375232-G-T

2305593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375255-T-A

2305620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375277-A-G

2305686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375325-C-T

2305757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375402-G-C

2305789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375435-T-C

2305803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375449-G-A

2305803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34375449-G-C

2319038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34381267-G-A

2319038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34381267-G-T

http://identifiers.org/hco/4/GRCh38#2319054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34381283-C-A

http://identifiers.org/hco/4/GRCh38#2319064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34381293-C-A

2319064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34381293-C-T

2319085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34381306-T-A

2319085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34381306-T-C

2319107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381323-T-C

2319107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381323-T-G

http://identifiers.org/hco/4/GRCh38#2319114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34381330-C-A

2319114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381330-C-T

2319152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381368-C-T

2319154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381370-T-C

2319203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381421-T-C

2319448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381685-C-T

2319578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34381820-G-A

http://identifiers.org/hco/4/GRCh38#2319657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34381900-A-C

2319901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382056-G-C

http://identifiers.org/hco/4/GRCh38#2320047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34382196-C-A

http://identifiers.org/hco/4/GRCh38#2320064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34382212-C-A

2320064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382212-C-G

2320064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382212-C-T

2320100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382226-T-A

2320100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382226-T-C

2320100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382226-T-G

2320128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382241-T-A

2320128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382241-T-C

2320193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous variant
orthologous variants: 34382319-G-A

2320295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382421-G-A

2320324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382452-C-T

2320354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382482-A-G

2320361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382493-G-A

2320361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382493-G-C

2320361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382493-G-T

2320367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382499-T-C

2320367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382499-T-G

2320454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382584-G-A

2320514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382639-G-A

2320725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382811-C-T

2320823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382886-G-C

2320823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382886-G-T

2320914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34382953-C-T

2320966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34383034-C-T

2321188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34383177-G-T

http://identifiers.org/hco/4/GRCh38#2321216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34383203-A-C

2329775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34385850-T-A

2329921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34385984-A-T

2329946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34386009-C-T

2330013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34386064-G-A

2330013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34386064-G-C

2330037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34386088-T-G

2333640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: 34387919-G-A

2334035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388263-A-T

2334178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388395-G-A

2334178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388395-G-C

2334218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388438-G-A

2334301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388507-G-C

2334334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388542-C-G

2334334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388542-C-T

2334739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388819-C-G

2334921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388886-G-A

2334921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388886-G-C

2335036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388965-G-A

2335065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34388991-T-G

2335085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389011-G-A

2335123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389048-A-G

2335140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389067-C-T

2335464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389321-C-T

2335472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389329-A-G

2335618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389467-G-T

2335749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 34389542-G-A

2335749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, stop_gained
orthologous variants: 34389542-G-T

http://identifiers.org/hco/4/GRCh38#2335767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34389560-C-A

2335767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 34389560-C-T

2335848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389622-A-G

2335848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389622-A-T

2335855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389629-A-G

2335869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389650-A-G

2335886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389667-T-C

2335892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389673-T-C

2336091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34389865-A-G

http://identifiers.org/hco/4/GRCh38#2336167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34389933-C-A

2336375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390143-A-G

2336595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390299-T-A

2337221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390548-C-T

2337257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390587-T-A

2337257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390587-T-C

2337257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390587-T-G

http://identifiers.org/hco/4/GRCh38#2337392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34390635-C-A

2337392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390635-C-T

2337398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34390640-T-C

2337490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous variant
orthologous variants: 34390732-G-A

2338247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391168-G-A

2338247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391168-G-T

2339173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391371-C-T

2339221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391423-G-A

2339245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391451-G-C

2339348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391514-C-T

2339381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391546-G-A

2339381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391546-G-T

http://identifiers.org/hco/4/GRCh38#2339395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34391560-C-A

2339395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391560-C-G

http://identifiers.org/hco/4/GRCh38#2339399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34391564-C-A

2339399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391564-C-T

2339494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous variant
orthologous variants: 34391670-C-T

2339593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: synonymous variant
orthologous variants: 34391769-C-T

2339681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391858-G-A

2339681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391858-G-T

2339717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391884-G-A

2339717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391884-G-C

2339717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391884-G-T

http://identifiers.org/hco/4/GRCh38#2339739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34391912-A-C

2339739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391912-A-G

2339739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34391912-A-T

2340185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392120-A-G

2340215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392159-C-T

2340216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392160-G-A

http://identifiers.org/hco/4/GRCh38#2340388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34392323-C-A

2340388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392323-C-T

2340614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392538-T-A

2340643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392558-G-A

2340718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392642-G-A

http://identifiers.org/hco/4/GRCh38#2340909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34392807-C-A

2340909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392807-C-G

2340909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392807-C-T

2340975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392892-G-A

2340983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392918-G-A

2341009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34392944-A-G

2341125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393027-C-G

http://identifiers.org/hco/4/GRCh38#2341143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34393045-C-A

2341143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393045-C-G

2341143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393045-C-T

2341159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393056-T-C

2341210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393100-T-A

2341210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393100-T-C

2341215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393105-G-A

2341215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393105-G-T

http://identifiers.org/hco/4/GRCh38#2341219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34393109-C-A

http://identifiers.org/hco/4/GRCh38#2341321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34393211-C-A

http://identifiers.org/hco/4/GRCh38#2341332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34393222-C-A

http://identifiers.org/hco/4/GRCh38#2341345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34393240-C-A

2341345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393240-C-T

2341348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393243-A-G

2341348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393243-A-T

2341353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393248-G-A

2341353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393248-G-T

2341379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393274-G-A

2341379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393274-G-T

2341380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393275-G-A

2341380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34393275-G-T

http://identifiers.org/hco/4/GRCh38#2341441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34393312-A-C

2342283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34394439-A-G

2348133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34395722-G-A

2348151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34395740-A-G

2348221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34395792-T-G

http://identifiers.org/hco/4/GRCh38#2348453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34396010-C-A

2348879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34396535-C-T

2349087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34396661-G-A

2349151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34396724-T-G

http://identifiers.org/hco/4/GRCh38#2349379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34396973-A-C

2349379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34396973-A-G

2349648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34397095-C-T

2349732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34397165-A-T

2352495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399132-G-A

2352499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399136-C-T

2352515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399151-G-C

2352546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399168-G-A

2352622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399240-C-T

2352869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399444-C-T

2352895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399469-C-T

2353204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399778-A-G

2353311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399883-G-A

2353311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34399883-G-C

2353579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400132-G-A

2353709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400235-G-A

http://identifiers.org/hco/4/GRCh38#2353922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34400506-C-A

2353922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400506-C-T

2354011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34400595-G-A

2354011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34400595-G-T

2354105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400691-G-A

2354105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400691-G-C

2354105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400691-G-T

2354162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400780-G-A

2354162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400780-G-C

2354162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400780-G-T

http://identifiers.org/hco/4/GRCh38#2354220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34400834-C-A

2354220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34400834-C-T

2354916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34401257-T-C

2357277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34403649-G-A

2357394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34403759-C-T

2357447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34403811-G-A

2357447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34403811-G-C

http://identifiers.org/hco/4/GRCh38#2357448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34403812-C-A

2360391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34404420-A-T

2360469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34404540-C-T

2360493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34404576-C-T

2360513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34404596-A-G

2360819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34404901-C-T

http://identifiers.org/hco/4/GRCh38#2360843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34404928-C-A

2361394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406103-T-C

2361445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34406147-C-T

2361504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406214-C-T

2361591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34406284-G-A

2361592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34406285-C-T

2361901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406601-G-C

2362002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406714-C-T

2362129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406825-G-A

2362180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406870-C-G

2362288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34406979-G-C

2362630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34407257-G-A

2365349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: 34408176-T-G

2365355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: 34408177-C-T

http://identifiers.org/hco/4/GRCh38#2365375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34408198-C-A

2365423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408252-G-A

2365423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408252-G-T

2365457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408274-G-A

2365457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408274-G-C

2365532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408343-T-C

2365792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408564-G-A

2366017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408771-G-A

http://identifiers.org/hco/4/GRCh38#2366200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34408923-C-A

2366200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34408923-C-T

2366376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34409072-G-A

2366656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34409292-A-G

2366867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34409481-C-T

2366943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34409646-G-A

2367137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34409867-T-C

http://identifiers.org/hco/4/GRCh38#2384139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34415735-C-A

2384535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34416038-A-T

2384632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34416084-G-A

http://identifiers.org/hco/4/GRCh38#2384740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34416151-C-A

2388139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34424182-G-A

2388146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34424189-C-T

http://identifiers.org/hco/4/GRCh38#2388243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34424297-A-C

2388603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34424621-G-A

2388603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34424621-G-T

2392303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34428738-G-A

2392303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34428738-G-T

2392347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34428772-C-T

http://identifiers.org/hco/4/GRCh38#2392422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34428842-A-C

2392475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34428872-C-T

2392552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34428953-C-T

2392567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34428968-T-C

2392922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34429887-G-A

2392935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34429898-C-T

2393099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34430066-T-C

2393108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34430075-T-C

2393181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34430238-G-A

2393491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron_variant, undefined
orthologous variants: 34430530-G-T

http://identifiers.org/hco/4/GRCh38#2393749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34430788-A-C

2393778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34430811-G-T

2393876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34430928-A-G

2394213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431197-G-T

2394276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431252-T-C

2394416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431370-C-G

2394416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431370-C-T

2394520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431457-G-A

2394520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431457-G-C

2394548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431479-T-C

2394566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431497-G-C

2394566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431497-G-T

2394641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431565-C-G

2394641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431565-C-T

2394963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431824-T-G

2395047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34431892-C-T

2409223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34437148-T-C

2409303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34437218-C-T

2409618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34437501-T-C

2409928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34437755-C-T

2409986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34437822-C-T

2411134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34438573-G-A

2411213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34438622-C-T

2411214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34438623-A-G

http://identifiers.org/hco/4/GRCh38#2411249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34438654-C-A

2411249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34438654-C-T

2411491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34438894-T-C

2411600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439011-G-A

2411907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439410-A-G

2412054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439567-G-A

2412067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439578-G-C

2412455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439885-C-T

2412461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439891-C-T

2412533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34439997-A-G

2412633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440109-G-T

2412716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440193-G-A

2412846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440312-G-C

2412928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440398-G-A

2412973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440442-C-G

2413044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440507-G-A

2413161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34440595-C-T

2414592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34441758-G-T

http://identifiers.org/hco/4/GRCh38#2415523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34442406-A-C

2415534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34442418-C-T

2415583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34442459-A-G

2416024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34442906-G-C

2416047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34442938-C-G

2416047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34442938-C-T

2416049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34442940-C-G

2416734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444052-C-T

http://identifiers.org/hco/4/GRCh38#2416847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34444162-C-A

2416877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444192-C-T

2417084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444368-C-T

2417306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444605-G-C

2417328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444630-C-T

2417399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444687-G-C

2417580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444829-C-G

2417580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444829-C-T

http://identifiers.org/hco/4/GRCh38#2417647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34444884-C-A

2417686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444919-T-C

2417686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444919-T-G

2417790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34444999-G-A

2417843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445062-G-A

2417843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445062-G-T

2417876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445088-G-A

2418077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445233-G-A

http://identifiers.org/hco/4/GRCh38#2418174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34445325-A-C

2418174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445325-A-G

2418174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445325-A-T

http://identifiers.org/hco/4/GRCh38#2418187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34445339-A-C

2418187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445339-A-G

2418209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445362-G-A

2418209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445362-G-C

2418209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445362-G-T

http://identifiers.org/hco/4/GRCh38#2418219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34445372-C-A

2418219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445372-C-T

2418241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: intron variant
orthologous variants: 34445402-A-G

http://identifiers.org/hco/4/GRCh38#2418337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#34445495-C-A

2418469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5 prime UTR variant
orthologous variants: 34445622-G-A

2418469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5 prime UTR variant
orthologous variants: 34445622-G-T

2418526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29334
most severe consequence: 5 prime UTR variant
orthologous variants: 34445678-C-T