141515017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: non coding transcript exon variant
orthologous variants: 37976650-G-A

141515020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: non coding transcript exon variant
orthologous variants: 37976653-G-C

141515046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37976679-T-C

141515092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37976725-T-A

141515149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37976767-T-C

141515149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37976767-T-G

141515294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37976905-G-A

141515294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37976905-G-T

141515525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977136-T-C

141516097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977655-G-T

141516100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977670-T-A

141516100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977670-T-C

141516160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977731-A-G

http://identifiers.org/hco/5/GRCh38#141516225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37977799-C-A

141516249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977823-G-T

141516252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977826-T-G

141516278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977852-G-A

141516295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37977869-T-C

http://identifiers.org/hco/5/GRCh38#141516417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37977981-C-A

141516545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37978103-A-G

141516708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37978266-G-A

141516708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37978266-G-C

141516708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37978266-G-T

http://identifiers.org/hco/5/GRCh38#141516818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37978361-C-A

141516818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37978361-C-T

141517022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37978565-C-G

141517022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37978565-C-T

141517137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37978676-T-A

141517153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37978692-G-T

141517375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37979074-C-T

141518074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37979618-C-T

141518507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37980871-C-G

141518507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37980871-C-T

141519403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37981413-T-C

141521162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37982498-C-T

141521218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37982561-T-C

141522286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983626-C-G

141522493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983801-T-C

http://identifiers.org/hco/5/GRCh38#141522597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37983888-A-C

141522685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983932-G-C

141522685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37983932-G-T

141523004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984208-T-C

141523031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984235-T-A

141523031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37984235-T-C

http://identifiers.org/hco/5/GRCh38#141523991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37984471-C-A

141524643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37985068-G-A

141524643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37985068-G-C

141524643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37985068-G-T

141524648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37985073-A-G

141524691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37985119-C-T

141524703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 37985131-C-T

http://identifiers.org/hco/5/GRCh38#141524721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#37985145-C-A

141524721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 37985145-C-G

141524746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37985174-G-T

141524766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37985194-T-C

141525219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37985658-C-T

141525774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37986152-C-T

141526051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 37986369-T-C

141526147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 37986465-C-T

141526200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37986522-C-T

141526339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 37986639-T-C

141526500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37986794-A-G

141527102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987297-C-T

http://identifiers.org/hco/5/GRCh38#141527433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37987427-A-C

141527738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987675-G-A

141527738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987675-G-C

141527738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987675-G-T

http://identifiers.org/hco/5/GRCh38#141527745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37987682-C-A

141527769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987706-A-G

141528029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987949-G-A

141528029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37987949-G-C

141528390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37988403-G-A

141528390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 37988403-G-C

141528445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37988519-T-C

http://identifiers.org/hco/5/GRCh38#141528513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37988587-C-A

141528604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37988677-G-A

141528640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37988712-A-G

141528805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37988869-C-T

141528983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37989051-G-T

141529092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37989161-A-G

141529208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 37989263-A-G

141532080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37991041-C-T

141532160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37991114-G-A

141532847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37991670-C-T

141533074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37992283-T-C

141534001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993195-A-G

141534035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993210-A-G

141534035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993210-A-T

141534054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993229-A-T

http://identifiers.org/hco/5/GRCh38#141534080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37993261-C-A

141534156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993331-T-C

141534226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993361-G-T

141534258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993392-C-G

141534258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993392-C-T

141534294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993425-T-C

http://identifiers.org/hco/5/GRCh38#141534423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37993556-A-C

141534423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37993556-A-G

141534460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37993591-T-C

141534482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37993613-G-A

141534482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37993613-G-T

141534517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993647-G-A

141534517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993647-G-T

141534526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993655-C-T

141534646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37993747-A-G

141535009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994124-C-T

http://identifiers.org/hco/5/GRCh38#141535430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#37994498-C-A

141535728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37994786-A-G

141536597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37995558-G-T

141555378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38008226-G-C

141555933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38008768-C-T

141555934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38008769-G-A

141555947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38008782-G-C

141556164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38008983-A-G

141556505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38009295-T-C

141556651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38009399-T-C

http://identifiers.org/hco/5/GRCh38#141557363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38009831-C-A

http://identifiers.org/hco/5/GRCh38#141557650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38010210-C-A

141557699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38010258-T-A

141557869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38010417-C-T

http://identifiers.org/hco/5/GRCh38#141558341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38010880-C-A

141558341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38010880-C-G

141558347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38010886-A-G

141558646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011206-G-A

141558667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011220-C-T

141559353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38011935-G-A

141559442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012022-C-T

http://identifiers.org/hco/5/GRCh38#141559447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38012027-C-A

141559448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012028-A-T

141559530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012089-T-C

141559648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012202-C-T

141559748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012294-C-T

141560310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012822-T-A

141560348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012838-C-G

141560446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38012920-C-T

141560621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013045-G-C

141560668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38013091-C-T

141560845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013257-G-A

141560845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013257-G-C

141560845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013257-G-T

141560883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013295-T-A

141560883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013295-T-G

141560975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013378-C-G

141560975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013378-C-T

141560977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013380-G-C

141560977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38013380-G-T

141561185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013584-T-C

141561364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013742-G-T

141561376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013754-T-C

141561388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38013766-T-G

141561758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014089-C-T

141561765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014096-C-T

http://identifiers.org/hco/5/GRCh38#141561911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38014376-C-A

141561911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014376-C-T

141561919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014384-T-C

http://identifiers.org/hco/5/GRCh38#141562022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38014494-C-A

http://identifiers.org/hco/5/GRCh38#141562037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38014508-C-A

141562198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014651-T-C

141562210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014664-G-T

141562366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014783-T-C

141562372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014789-C-T

141562569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014973-T-C

141562569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38014973-T-G

http://identifiers.org/hco/5/GRCh38#141562620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38015029-C-A

141562778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015121-A-T

141562934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015263-A-G

141562935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015264-T-A

http://identifiers.org/hco/5/GRCh38#141563000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38015312-A-C

141563017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015329-T-A

141563017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38015329-T-C

141563139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38015396-T-C

141563140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38015397-C-T

141563172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38015431-G-C

141563304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38015565-G-A

141563318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38015589-G-C

141563383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38015648-G-T

141563998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38016375-G-A

141563998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38016375-G-T

141563999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38016376-G-T

http://identifiers.org/hco/5/GRCh38#141564062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38016441-C-A

141564063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38016442-T-A

http://identifiers.org/hco/5/GRCh38#141564163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38016541-C-A

141564270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016655-T-C

http://identifiers.org/hco/5/GRCh38#141564429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38016813-C-A

141564512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016896-T-A

141564512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016896-T-C

http://identifiers.org/hco/5/GRCh38#141564513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#38016897-C-A

141564521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016905-A-G

141564556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016939-G-A

141564556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016939-G-T

141564562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016945-G-T

141564582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38016966-T-C

141564624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38017008-G-A

141564624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38017008-G-T

141564770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38017147-G-C

141564770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38017147-G-T

http://identifiers.org/hco/5/GRCh38#141564848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38017233-C-A

http://identifiers.org/hco/5/GRCh38#141565214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38017610-C-A

141565377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38017743-T-C

141567333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38019767-T-C

141567465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38019876-G-A

141567540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38019945-G-A

141567683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38020207-T-C

141567761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38020280-G-C

141568704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38020728-T-A

141570950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38021902-T-C

141571393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022233-A-G

141571673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022515-T-C

141571730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022565-C-T

141571750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022585-C-T

141571751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022586-C-T

141571853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022681-G-A

141571869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022697-T-A

141571869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022697-T-C

141571930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38022755-G-A

http://identifiers.org/hco/5/GRCh38#141571939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38022764-A-C

141571974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38022799-T-C

141572056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022881-G-A

141572056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022881-G-C

141572056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38022881-G-T

141572199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38023023-A-G

141572875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38023250-T-C

141572974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38023354-T-C

141573091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: intron variant
orthologous variants: 38023460-G-A

141573738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023740-A-G

141573738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023740-A-T

141573741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023743-T-A

141573741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023743-T-G

141573855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023854-T-G

141573864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023863-G-A

141573864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023863-G-C

141573864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023863-G-T

141573902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38023901-T-C

http://identifiers.org/hco/5/GRCh38#141573905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38023904-C-A

141573905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38023904-C-G

141573905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38023904-C-T

141573921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023920-A-G

141573942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: synonymous variant
orthologous variants: 38023941-A-G

http://identifiers.org/hco/5/GRCh38#141573946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38023945-C-A

141573946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38023945-C-T

141574019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38024027-G-A

141574025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38024033-G-A

141574025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: missense variant
orthologous variants: 38024033-G-T

141574125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38024145-A-G

141574315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38024329-G-T

http://identifiers.org/hco/5/GRCh38#141574889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38024745-C-A

141574889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38024745-C-G

141574889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38024745-C-T

141574892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38024748-G-A

141574941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38024820-T-C

141575120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38024999-A-G

141575164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025050-C-G

141575239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025103-T-A

141575240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025104-G-A

141575240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025104-G-C

141575240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025104-G-T

141575736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025573-T-C

141575793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025639-A-G

141575873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38025840-A-G

141575914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38026006-T-C

141576017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38026119-C-T

http://identifiers.org/hco/5/GRCh38#141576181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38026268-C-A

141576181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38026268-C-G

141576430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38026619-G-A

141576430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38026619-G-T

141576617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38027024-G-A

141576617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38027024-G-T

141576711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38027099-G-T

141576717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38027105-A-G

http://identifiers.org/hco/5/GRCh38#141577079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38027484-C-A

141577439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028204-T-C

141577461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028220-G-A

141577461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028220-G-T

141577573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38028333-A-G

141577697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028448-T-C

http://identifiers.org/hco/5/GRCh38#141577711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38028462-C-A

141577711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028462-C-G

141577711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028462-C-T

141577838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028541-T-C

141577879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028577-G-A

141577879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38028577-G-T

141578022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38028775-A-T

141578209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38029126-G-A

141578209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38029126-G-C

141578209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38029126-G-T

141578440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38029340-T-A

141578440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38029340-T-C

141578440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38029340-T-G

141578616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38029515-G-C

141578650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38029549-A-G

141578707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38029605-T-C

141578795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38029677-G-A

141579238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38030693-G-A

141579238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38030693-G-T

141579526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38030977-T-C

141579878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38031373-G-T

http://identifiers.org/hco/5/GRCh38#141579939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38031410-C-A

141580125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38031474-G-C

141580141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38031479-T-C

141580446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38031765-G-A

141580604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38033560-T-C

http://identifiers.org/hco/5/GRCh38#141580758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38033712-C-A

141580758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38033712-C-T

141580773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 38033727-A-G

141580841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, synonymous_variant
orthologous variants: 38033795-G-A

141580841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 38033795-G-C

http://identifiers.org/hco/5/GRCh38#141580900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38033853-C-A

141581386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38034340-G-A

141581408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38034357-G-A

141581408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38034357-G-C

141581810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38034638-T-A

141581810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38034638-T-C

141581930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 38034773-G-A

141581930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 38034773-G-C

141581930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 38034773-G-T

141581955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 38034797-G-A

141581974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 38034814-G-A

141581974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 38034814-G-T

141582002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 38034844-G-A

141582169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38034993-G-T

141582182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035009-A-G

http://identifiers.org/hco/5/GRCh38#141582235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38035056-C-A

141582235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035056-C-G

141582235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035056-C-T

141582410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035236-T-C

141582436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035270-A-G

141582441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035275-G-A

141582441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035275-G-T

141582536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035372-C-T

141582950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38035957-A-G

http://identifiers.org/hco/5/GRCh38#141583059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38036019-C-A

141583349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38036259-A-G

141583414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38036319-T-C

141583547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38036442-C-T

141583619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 38036514-G-C

http://identifiers.org/hco/5/GRCh38#141584015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38036708-A-C

141584015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38036708-A-G

141584024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38036717-T-G

141584088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38036778-G-T

141584238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38036923-G-A

141584238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38036923-G-T

141586560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037580-G-A

141586586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037606-T-G

141586734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037757-T-A

141586848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037869-G-A

141586937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037925-G-A

141586937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037925-G-C

141586937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38037925-G-T

141586998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38038010-T-A

141587006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38038022-C-T

141587063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38038078-C-T

141587117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38038132-A-G

141587225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38038239-T-C

141587225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38038239-T-G

http://identifiers.org/hco/5/GRCh38#141587259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38038288-C-A

141587259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38038288-C-G

141587471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38038667-T-C

141587574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38038768-T-C

141587621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38038819-C-T

141587915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38039105-C-T

141588028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38039226-C-T

141588100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38039271-G-A

141588100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38039271-G-T

141588111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38039285-T-C

141588111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 38039285-T-G

141588172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38039389-A-G

141588267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38039486-A-G

141588299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38039520-G-A

141588299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38039520-G-T

141588302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38039523-C-T

141588336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38039558-A-G

141589576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38040396-T-C

141589664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38040474-T-C

141589693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38040503-G-A

141592076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38041165-T-A

141592076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38041165-T-C

141592827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38042186-T-C

141596867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38049442-G-A

141596878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38049431-T-C

141597103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38049201-G-A

141597328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048998-A-G

141597358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048995-G-C

141597496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048873-G-A

141597545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048828-G-T

141597605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048767-G-A

141597605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048767-G-C

141597628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048648-T-A

141597710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38048530-T-C

141597868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38050699-C-T

141598018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38050837-C-T

141598165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38050974-T-G

141598374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38051161-T-C

141598631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38051394-T-C

141598631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38051394-T-G

141598661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38051424-T-C

141598674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38051658-G-A

141599053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38052205-A-G

141599061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38052213-G-A

141601688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38055113-G-T

141601778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38055189-T-C

141604208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38057016-G-C

141604233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38057037-C-G

141606137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38059369-C-T

141606914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38060059-T-A

141607120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38060191-T-C

141607210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38060278-C-T

http://identifiers.org/hco/5/GRCh38#141607683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38060806-C-A

141608489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38061499-C-G

http://identifiers.org/hco/5/GRCh38#141608768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38061845-A-C

141608922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38061989-T-C

141609005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38062078-G-A

141609963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38062972-A-G

141613627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38063966-G-A

141613627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38063966-G-T

141614115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38064543-T-C

141614288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38064708-T-C

141616835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38066355-A-G

http://identifiers.org/hco/5/GRCh38#141617193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#38066738-C-A

141617776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38067253-C-T

141617962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 38067448-G-C

141618291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 38067750-G-A

141618291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 38067750-G-C

141618291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 38067750-G-T

141618319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 38067770-G-A

141618319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 38067770-G-T

141618406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 38067850-T-G

141618541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38067989-G-A

141618541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38067989-G-C

141618541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38067989-G-T

141618765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38068220-G-A

141618765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2876
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38068220-G-T