6451390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938482-T-C

6451541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938620-T-C

6451541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938620-T-G

http://identifiers.org/hco/17/GRCh38#6451627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71938704-C-A

6451627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938704-C-T

http://identifiers.org/hco/17/GRCh38#6451632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71938709-C-A

6451632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938709-C-G

6451632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938709-C-T

http://identifiers.org/hco/17/GRCh38#6451674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71938742-C-A

6451674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938742-C-T

6451702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71938772-G-A

http://identifiers.org/hco/17/GRCh38#6451991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71939093-C-A

6451991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939093-C-T

6452014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939119-C-T

http://identifiers.org/hco/17/GRCh38#6452340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71939423-A-C

6452356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939438-A-G

http://identifiers.org/hco/17/GRCh38#6452548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71939626-C-A

http://identifiers.org/hco/17/GRCh38#6452594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71939662-C-A

6452700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939713-A-G

6452700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939713-A-T

http://identifiers.org/hco/17/GRCh38#6452703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71939716-C-A

6452703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939716-C-T

6452739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939751-C-G

6453300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71939983-G-T

6453462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940113-G-C

6453462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940113-G-T

6453463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940114-G-T

http://identifiers.org/hco/17/GRCh38#6453491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71940142-C-A

6453491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940142-C-G

6453491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940142-C-T

6453493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940145-G-C

6453493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940145-G-T

6453498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940150-G-A

6453498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940150-G-C

6453498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940150-G-T

6453596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940285-T-C

6453626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940314-G-A

6453626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940314-G-T

6453690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940382-G-A

6453763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940456-G-T

6453847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940508-G-A

6453847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940508-G-T

6454115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940743-G-A

6454409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71940981-G-A

6454471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941037-C-T

6455000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941549-G-A

6455000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941549-G-T

http://identifiers.org/hco/17/GRCh38#6455052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71941598-C-A

6455052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941598-C-T

http://identifiers.org/hco/17/GRCh38#6455056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71941602-C-A

6455056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941602-C-T

http://identifiers.org/hco/17/GRCh38#6455137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71941687-C-A

6455137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941687-C-T

6455258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941809-G-A

6455258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941809-G-C

6455258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941809-G-T

http://identifiers.org/hco/17/GRCh38#6455309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71941859-C-A

6455309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941859-C-G

6455309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3 prime UTR variant
orthologous variants: 71941859-C-T

6455602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71942145-C-T

6455605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71942148-C-T

6455626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71942169-G-A

6455626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 71942169-G-T

6455886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942278-C-T

6457271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942424-C-T

6457377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942506-C-T

6457391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942520-A-G

6457444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942570-G-A

http://identifiers.org/hco/17/GRCh38#6457702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71942775-C-A

6457702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71942775-C-T

6457754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942826-G-A

6457754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942826-G-C

6457754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71942826-G-T

http://identifiers.org/hco/17/GRCh38#6457875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71942908-C-A

6459191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944079-C-G

6459305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944189-G-T

http://identifiers.org/hco/17/GRCh38#6459379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71944255-A-C

6459379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944255-A-T

6459730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944590-C-T

http://identifiers.org/hco/17/GRCh38#6459882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71944749-C-A

6459882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944749-C-T

6459933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944796-G-A

http://identifiers.org/hco/17/GRCh38#6459990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71944844-A-C

6460053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944908-C-T

6460108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944962-T-G

6460145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71944999-A-T

6460522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71946163-G-A

6460895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71946509-T-C

http://identifiers.org/hco/17/GRCh38#6461127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71946702-A-C

http://identifiers.org/hco/17/GRCh38#6461284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71946834-C-A

6461284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71946834-C-T

http://identifiers.org/hco/17/GRCh38#6461433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71947016-A-C

6461433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71947016-A-G

6461433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71947016-A-T

6461561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71947144-T-C

6461688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947249-G-T

http://identifiers.org/hco/17/GRCh38#6461707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71947268-C-A

6461707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947268-C-T

6461970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71947431-C-T

6462330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71947793-G-A

6462374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71947825-C-T

6462764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71948133-A-G

6462778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71948150-G-A

6462959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71948276-A-G

6462966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71948281-C-T

6463443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71948601-G-A

http://identifiers.org/hco/17/GRCh38#6463472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71948623-A-C

6463472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 71948623-A-G

http://identifiers.org/hco/17/GRCh38#6463612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71948721-C-A

6463612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 71948721-C-T

6463632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 71948741-T-C

6463645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71948754-G-A

6463645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71948754-G-T

http://identifiers.org/hco/17/GRCh38#6463646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71948755-C-A

6463646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 71948755-C-T

6463650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948759-T-A

6463674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948790-A-G

6463677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948793-G-C

6463677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71948793-G-T

6463743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71948857-C-T

6463818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71948932-C-T

6463944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949036-G-A

6463944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949036-G-T

6464100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949138-C-G

6464100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949138-C-T

6464292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71949334-T-C

http://identifiers.org/hco/17/GRCh38#6464583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71949596-C-A

6464583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949596-C-T

6465097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949875-G-A

6465165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949907-G-C

6465312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71949975-C-T

6465506-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950145-T-A

6465691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950333-T-C

6465697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950339-A-G

6465823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950441-G-A

6465823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950441-G-C

6466336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950846-A-T

6466506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71950983-C-T

6466897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951209-T-A

http://identifiers.org/hco/17/GRCh38#6467235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71951363-C-A

6467235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951363-C-T

6467497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951633-A-G

6467535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951676-A-G

6467638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951780-T-C

6467665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951809-C-T

http://identifiers.org/hco/17/GRCh38#6467766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71951905-C-A

6467766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71951905-C-T

6468032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952162-G-A

6468108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952203-T-C

6468108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952203-T-G

6468127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952225-G-A

6468127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952225-G-T

http://identifiers.org/hco/17/GRCh38#6468154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71952252-C-A

6468299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71952374-G-A

6468302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71952377-G-A

6468303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71952378-G-A

6468430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952514-G-A

6468430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952514-G-T

6468434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952518-G-A

6468434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952518-G-T

6468483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952536-G-A

6468483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952536-G-T

6468757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952783-G-A

6468776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952802-C-T

http://identifiers.org/hco/17/GRCh38#6468922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71952904-C-A

6468922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952904-C-T

6468925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952907-C-G

6468925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71952907-C-T

6469138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71953094-C-T

6469187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71953137-C-T

http://identifiers.org/hco/17/GRCh38#6469235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71953185-C-A

6469235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71953185-C-G

6470047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71953738-C-T

http://identifiers.org/hco/17/GRCh38#6470185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71953866-C-A

6470246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71953907-T-G

6470350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71954011-G-A

6470559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954187-G-A

6470559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954187-G-C

6470559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954187-G-T

6470629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954252-A-G

6470837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954460-G-C

6470894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954552-A-G

6470957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954650-C-T

6471001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954713-G-A

6471149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71954877-G-A

http://identifiers.org/hco/17/GRCh38#6471183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71954911-C-A

6471227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71954955-C-T

6471300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71955028-G-A

http://identifiers.org/hco/17/GRCh38#6471389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71955117-C-A

6471389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955117-C-T

http://identifiers.org/hco/17/GRCh38#6471420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71955148-C-A

6471420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955148-C-T

6471485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955197-G-A

6471485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955197-G-T

6471945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955589-G-A

6472053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 71955707-C-T

6472258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71955879-C-G

6472482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956105-C-G

6472580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956208-T-C

6472580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956208-T-G

http://identifiers.org/hco/17/GRCh38#6472586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71956214-C-A

6472610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956247-G-A

6472865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956504-A-G

6472902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956529-T-G

6472956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71956583-C-T

6473073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957114-T-A

6473073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957114-T-C

http://identifiers.org/hco/17/GRCh38#6473102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71957141-C-A

6473102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957141-C-T

http://identifiers.org/hco/17/GRCh38#6473200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71957240-C-A

http://identifiers.org/hco/17/GRCh38#6473201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71957241-C-A

6473201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 71957241-C-G

http://identifiers.org/hco/17/GRCh38#6473236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71957276-C-A

6473305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957306-G-T

http://identifiers.org/hco/17/GRCh38#6473314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71957315-C-A

6473435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957419-C-G

6474109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957682-G-C

6474113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957686-G-A

6474220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957777-A-G

6474307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957849-A-G

6474307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957849-A-T

6474419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71957920-A-T

6474481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71957981-T-A

http://identifiers.org/hco/17/GRCh38#6474559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71958059-A-C

6474563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71958063-G-A

6474675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958144-C-T

6474704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958172-G-A

6474704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958172-G-T

6474734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958202-A-G

6474876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958355-C-T

http://identifiers.org/hco/17/GRCh38#6475088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71958548-A-C

6475105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958565-G-C

6475213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958692-C-G

6475389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958832-G-C

6475486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958957-T-G

6475531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71958997-T-C

6475979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960199-C-T

6476159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960378-G-A

6476159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960378-G-T

6476394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960579-G-A

6476412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960597-T-G

6476567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960708-G-C

6476812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960929-G-A

6476893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71960974-G-T

6476955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71961035-A-G

6477064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71961164-G-A

6477064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 71961164-G-C

6477399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71961449-C-T

6477905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71961620-C-T

6477919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71961634-G-A

6477919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71961634-G-T

6478413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71962105-T-G

6478506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71962192-G-A

6478506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71962192-G-C

6478506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 71962192-G-T

6478631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 71962309-A-G

6478866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962521-A-G

6478866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962521-A-T

http://identifiers.org/hco/17/GRCh38#6479069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71962686-C-A

http://identifiers.org/hco/17/GRCh38#6479070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71962687-C-A

6479106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962718-G-A

6479106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962718-G-T

6479155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962768-T-C

http://identifiers.org/hco/17/GRCh38#6479195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71962807-C-A

http://identifiers.org/hco/17/GRCh38#6479232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71962821-C-A

6479232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962821-C-T

6479243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962832-A-G

6479333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962909-A-G

6479399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71962957-C-T

6479538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963071-C-T

6479544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963077-G-C

6479544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963077-G-T

6479549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963082-G-T

http://identifiers.org/hco/17/GRCh38#6479576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71963108-C-A

6479576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963108-C-T

6479599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963132-G-A

6479599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963132-G-T

6479647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963176-C-T

6479652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963181-T-A

6479652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963181-T-C

6479690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963219-A-G

6479850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963381-G-T

6479865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963396-T-C

6480148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963756-G-A

6480245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963854-C-T

6480389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71963988-G-A

6480437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964035-T-C

6480478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964060-T-C

6480624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964130-T-C

6480737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964234-G-A

http://identifiers.org/hco/17/GRCh38#6480802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71964298-C-A

6480802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964298-C-T

http://identifiers.org/hco/17/GRCh38#6480869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71964360-C-A

6480869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964360-C-T

6480876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964367-A-G

6480913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964406-T-C

6480950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964450-A-G

6481004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71964499-A-G

6483293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965038-T-C

6483886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965546-A-G

6483891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965551-G-A

6483899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965559-G-T

6484079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965664-G-A

6484079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965664-G-T

http://identifiers.org/hco/17/GRCh38#6484104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71965690-C-A

6484104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965690-C-G

6484104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965690-C-T

http://identifiers.org/hco/17/GRCh38#6484170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71965754-C-A

6484170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965754-C-T

6484206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965775-C-T

6484430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71965988-A-G

6484461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71966020-A-G

6485029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71966503-G-C

6485459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967032-A-G

http://identifiers.org/hco/17/GRCh38#6485608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71967240-A-C

6485615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967247-G-A

6485618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967249-G-A

6485641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967252-C-T

6485997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967561-T-C

6486223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967779-A-G

6486266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71967809-G-T

6486517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71968035-T-C

6486632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71968163-G-C

6486702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71968702-C-T

6487087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969217-G-T

6487271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969418-G-T

6487307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969461-G-A

6487424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969564-G-C

6487458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969605-G-A

6487500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969640-C-T

http://identifiers.org/hco/17/GRCh38#6487607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71969746-C-A

6487657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71969796-C-T

http://identifiers.org/hco/17/GRCh38#6487927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71970060-C-A

6487927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71970060-C-T

6487998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71970127-G-A

6488176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71970566-T-C

6488333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71970713-A-G

6488698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971086-G-A

6488919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971283-T-G

6488970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971333-C-T

6488976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971339-C-T

6489253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971615-A-G

6489256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971618-G-A

6489313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71971670-C-T

6494637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71974883-C-T

6494949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71975170-T-A

6495031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71975250-A-G

6495073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71975291-T-A

6495601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71975845-C-G

6495605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71975851-C-T

6495638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71975883-G-A

6496460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71976621-C-T

6496925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71977598-T-C

6496967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71977621-C-T

6497205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71977839-C-T

6497479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71978049-G-T

6497609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71978165-T-G

6497648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71978195-C-T

6497809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71978323-G-A

6497810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71978324-G-A

6498316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979014-C-T

6498432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979136-G-T

6498476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979176-C-T

6498688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979362-G-T

6498701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979375-G-T

6498709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979383-G-A

6498709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979383-G-C

6498712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979386-A-G

http://identifiers.org/hco/17/GRCh38#6498850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71979517-C-A

6499114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979776-C-T

6499227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71979860-G-A

6499529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71980388-T-A

http://identifiers.org/hco/17/GRCh38#6500334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71980685-A-C

6500334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71980685-A-G

http://identifiers.org/hco/17/GRCh38#6502587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71982188-C-A

6502637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982238-A-T

6502652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982254-G-A

6502715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982310-C-T

http://identifiers.org/hco/17/GRCh38#6502790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71982361-C-A

6502895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982442-T-G

http://identifiers.org/hco/17/GRCh38#6502930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71982471-A-C

6502940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982481-G-A

6502944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982485-C-T

6503013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982649-G-A

6503022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982673-T-C

6503048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71982756-T-A

6503211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983072-G-A

http://identifiers.org/hco/17/GRCh38#6503381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71983213-C-A

6503381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983213-C-T

http://identifiers.org/hco/17/GRCh38#6503481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71983308-C-A

6503481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983308-C-G

6503481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983308-C-T

6503516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983343-G-T

6503564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: synonymous variant
orthologous variants: 71983391-G-A

6503564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: synonymous variant
orthologous variants: 71983391-G-T

6503591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983416-G-C

6503591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983416-G-T

http://identifiers.org/hco/17/GRCh38#6503595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71983420-C-A

6503595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983420-C-T

6503615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983443-T-A

6503625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983454-C-G

6503625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983454-C-T

6503642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983471-A-T

6503676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983500-G-A

6503676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983500-G-C

http://identifiers.org/hco/17/GRCh38#6503699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71983522-C-A

6503719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983541-G-A

6503719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983541-G-C

6503719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983541-G-T

http://identifiers.org/hco/17/GRCh38#6503720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71983542-C-A

6503920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983740-G-A

6504131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71983944-G-A

6504289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71984055-C-T

6504475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71984172-T-A

6504708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71984381-T-G

6504834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71984469-T-C

6504882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71984515-T-C

6504882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71984515-T-G

6505518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71985007-C-T

6505519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71985008-G-A

6505519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71985008-G-T

6505641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71985122-A-G

6506033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71985466-G-C

6506072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71985483-G-C

6508853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71986935-C-T

6509128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71987300-C-T

6509141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71987313-G-C

6509355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71987573-C-T

6509390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71987608-G-A

6509826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71987941-C-T

6509847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71987962-C-T

http://identifiers.org/hco/17/GRCh38#6509954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71988068-C-A

6509954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71988068-C-T

http://identifiers.org/hco/17/GRCh38#6510472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71988430-C-A

6510472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71988430-C-T

http://identifiers.org/hco/17/GRCh38#6510513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71988471-C-A

6510513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71988471-C-T

http://identifiers.org/hco/17/GRCh38#6510518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71988476-C-A

http://identifiers.org/hco/17/GRCh38#6510687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71988612-C-A

6510767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71988709-T-G

6511578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989497-C-T

http://identifiers.org/hco/17/GRCh38#6511671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71989603-C-A

6511677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989609-G-C

6511681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989613-G-A

6511799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989655-T-C

6512120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989769-G-A

6512120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989769-G-T

6512130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71989779-G-A

6512605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71990234-G-C

6512786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71990405-A-G

6513063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71990647-A-G

6513084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71990666-A-G

6513391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71991127-T-C

http://identifiers.org/hco/17/GRCh38#6513511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71991285-A-C

6515608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71994490-G-C

6518343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71996136-G-T

6518371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71996165-C-T

http://identifiers.org/hco/17/GRCh38#6518393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71996188-C-A

6518779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71996461-A-G

http://identifiers.org/hco/17/GRCh38#6518916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71996598-A-C

6518962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71996642-T-C

6520791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71999276-G-A

http://identifiers.org/hco/17/GRCh38#6521039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71999488-C-A

6521048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71999497-G-T

http://identifiers.org/hco/17/GRCh38#6521071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71999517-C-A

6521071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71999517-C-T

http://identifiers.org/hco/17/GRCh38#6521160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71999531-C-A

6521160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 71999531-C-T

http://identifiers.org/hco/17/GRCh38#6521164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71999535-C-A

6521435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71999569-T-C

6521501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71999631-C-T

http://identifiers.org/hco/17/GRCh38#6521671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#71999720-A-C

6521720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 71999770-A-G

6522064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72000238-C-G

6522134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72000307-C-T

6522152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72000329-C-T

6522153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72000330-G-A

6522391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72000766-G-C

6522480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72000852-G-A

6523025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72001297-A-G

6523098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72001359-T-A

6523615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, undefined
orthologous variants: 72001851-A-G

http://identifiers.org/hco/17/GRCh38#6523645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#72001883-A-C

6523645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, undefined
orthologous variants: 72001883-A-G

6523717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72001957-G-A

6523717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72001957-G-C

6524064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72002203-C-G

6524140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72002281-C-G

6525208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72002998-G-A

6525208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72002998-G-T

6525261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003017-G-T

http://identifiers.org/hco/17/GRCh38#6525304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72003037-C-A

6525304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003037-C-G

6525304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003037-C-T

6525347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003074-G-C

6525361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, missense_variant
orthologous variants: 72003088-T-G

6525369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 72003096-C-T

6525487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003213-C-T

6525496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003222-G-A

6525496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003222-G-T

6525552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003359-T-G

6525670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003482-G-A

6526199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72003977-T-C

6526231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72004009-T-C

6526340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72004117-G-T

6526485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72004258-A-G

6526896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005349-G-T

http://identifiers.org/hco/17/GRCh38#6526925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72005380-A-C

6526963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005398-G-A

6526971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005406-T-G

6526972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005407-G-A

6527216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005671-G-A

6527587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005706-G-C

http://identifiers.org/hco/17/GRCh38#6527707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72005816-C-A

6527768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005874-T-G

6527833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005958-C-T

6527858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005982-C-T

6527864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72005988-G-A

6527884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72006004-G-A

http://identifiers.org/hco/17/GRCh38#6528209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72006037-A-C

http://identifiers.org/hco/17/GRCh38#6528217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72006045-C-A

http://identifiers.org/hco/17/GRCh38#6528312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72006067-C-A

6529789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72006922-A-G

6529790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72006923-C-T

6530057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72007143-G-A

6530369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72007428-C-T

6530647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72007555-C-G

http://identifiers.org/hco/17/GRCh38#6530784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72007654-A-C

6536280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009441-C-T

6536325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009499-G-C

6536527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009708-G-A

6536527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009708-G-T

6536528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009709-G-T

6536543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009724-G-A

6536695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72009895-G-A

6536862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72010049-G-A

6537926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72010852-T-A

http://identifiers.org/hco/17/GRCh38#6538043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72010969-C-A

6538043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: missense variant
orthologous variants: 72010969-C-T

6538122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72011047-T-C

6538179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72011101-T-A

http://identifiers.org/hco/17/GRCh38#6538201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72011123-C-A

6538201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72011123-C-T

http://identifiers.org/hco/17/GRCh38#6538210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72011132-C-A

6538210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72011132-C-T

6538496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72011365-A-G

6538709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72013111-C-T

6539075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72013385-C-T

6539191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72013497-T-C

6540067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72014636-G-A

6540382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72015028-C-T

6542727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72016251-G-A

6543476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72016728-A-G

6543476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72016728-A-T

6543670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72016897-G-A

6543770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72016996-G-A

6544006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72017199-G-A

6545783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72018646-C-T

6545817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72018674-G-A

6545864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72018720-C-T

6545865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72018721-A-G

6545921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72018763-C-T

http://identifiers.org/hco/17/GRCh38#6545976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72018817-C-A

6546027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72018867-G-C

6547536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72020136-A-G

6548092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72020354-C-T

6548487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72020740-G-T

6549304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72021337-T-G

6549354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72021381-G-A

6549446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72021429-T-C

http://identifiers.org/hco/17/GRCh38#6549797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#72021786-C-A

6549797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72021786-C-G

6549797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72021786-C-T

6551589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72022754-C-T

6553154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72023709-A-T

6553293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72023893-G-T

6553620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72024207-T-C

6553620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72024207-T-G

6555658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72025796-C-T

6555842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72025990-G-C

6556125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026262-C-T

6556276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026397-G-A

6556276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026397-G-C

6556276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026397-G-T

6556308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026429-G-A

6556308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026429-G-T

6556338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026447-G-A

6556338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026447-G-C

6556338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: intron variant
orthologous variants: 72026447-G-T

6556500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 5 prime UTR variant
orthologous variants: 72026590-G-A

6556500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 5 prime UTR variant
orthologous variants: 72026590-G-C

6556500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21043
most severe consequence: 5 prime UTR variant
orthologous variants: 72026590-G-T